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These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in
this section to the one reported in Genomic regions,
transcripts, and products above.
mRNA and Protein(s)
-
NM_001039083.5 → NP_001034172.3 ADP-ribosylation factor-like protein 17 isoform a
See identical proteins and their annotated locations for NP_001034172.3
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) encodes the longest isoform (a).
- Source sequence(s)
-
AC217777
- Consensus CDS
-
CCDS58557.1
- UniProtKB/Swiss-Prot
- B0AZR6, Q59FW5, Q8IVW1, Q8N6E2, Q8TD73, Q8WW54, Q9NZD5, Q9P158
- UniProtKB/TrEMBL
- A0A0G2JMH3, A8K0M5
- Related
- ENSP00000404247.4, ENST00000450673.4
- Conserved Domains (3) summary
-
- COG1100
Location:13 → 88
- Gem1; GTPase SAR1 family domain [General function prediction only]
- pfam15840
Location:115 → 176
- ARL17; ADP-ribosylation factor-like protein 17
- cl21455
Location:1 → 87
- P-loop_NTPase; P-loop containing Nucleoside Triphosphate Hydrolases
-
NM_001103154.2 → NP_001096624.1 ADP-ribosylation factor-like protein 17 isoform b
See identical proteins and their annotated locations for NP_001096624.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) uses an alternate exon in the 3' coding region, compared to variant 1. The encoded isoform (b) has a distinct and shorter C-terminus, compared to isoform a. Variants 2 and 4 encode the same isoform (b).
- Source sequence(s)
-
AC005829, AC217777, AI638797
- Consensus CDS
-
CCDS54137.1
- UniProtKB/Swiss-Prot
-
Q8IVW1
- Related
- ENSP00000459151.1, ENST00000570618.6
- Conserved Domains (1) summary
-
- cl21455
Location:1 → 88
- P-loop_NTPase; P-loop containing Nucleoside Triphosphate Hydrolases
-
NM_001330240.1 → NP_001317169.1 ADP-ribosylation factor-like protein 17 isoform c
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) uses an alternate exon in the 3' coding region, compared to variant 1. The encoded isoform (c) has a distinct and shorter C-terminus, compared to isoform a.
- Source sequence(s)
-
AC217777, CA420101
- UniProtKB/TrEMBL
- I3L1V5, I3L2E4
- Conserved Domains (2) summary
-
- COG1100
Location:13 → 85
- Gem1; GTPase SAR1 family domain [General function prediction only]
- cl21455
Location:1 → 86
- P-loop_NTPase; P-loop containing Nucleoside Triphosphate Hydrolases
-
NM_001352769.1 → NP_001339698.1 ADP-ribosylation factor-like protein 17 isoform b
Status: VALIDATED
- Description
- Transcript Variant: This variant (4) uses an alternate exon in the 3' coding region, compared to variant 1. The encoded isoform (b) has a distinct and shorter C-terminus, compared to isoform a. Variants 2 and 4 encode the same isoform (b).
- Source sequence(s)
-
AC005829, AC217777
- Consensus CDS
-
CCDS54137.1
- Related
- ENSP00000499587.1, ENST00000656849.1
- Conserved Domains (1) summary
-
- cl21455
Location:1 → 88
- P-loop_NTPase; P-loop containing Nucleoside Triphosphate Hydrolases
-
NM_001363805.1 → NP_001350734.1 ADP-ribosylation factor-like protein 17 isoform d
Status: VALIDATED
- Source sequence(s)
-
AC217777
- UniProtKB/TrEMBL
- A0A994J5X1, I3L3L1
- Related
- ENSP00000458681.2, ENST00000572991.6
- Conserved Domains (2) summary
-
- pfam15840
Location:115 → 176
- ARL17; ADP-ribosylation factor-like protein 17
- cl21455
Location:1 → 87
- P-loop_NTPase; P-loop containing Nucleoside Triphosphate Hydrolases
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000017.11 Reference GRCh38.p14 Primary Assembly
- Range
-
46274184..46361787 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060941.1 Alternate T2T-CHM13v2.0
- Range
-
47136194..47223769 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)