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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.
Genomic
-
NG_051248.1 RefSeqGene
- Range
-
5128..7738
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_001040025.3 → NP_001035114.2 ADP-ribosylation factor-like protein 16 isoform 1
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) encodes the longest isoform (1).
- Source sequence(s)
-
AC139530
- Consensus CDS
-
CCDS45813.2
- UniProtKB/Swiss-Prot
-
Q0P5N6
- UniProtKB/TrEMBL
-
B4E3H0
- Related
- ENSP00000483183.1, ENST00000622299.5
- Conserved Domains (1) summary
-
- cd00878
Location:1 → 166
- Arf_Arl; ADP-ribosylation factor(Arf)/Arf-like (Arl) small GTPases
-
NM_001329608.2 → NP_001316537.1 ADP-ribosylation factor-like protein 16 isoform 2
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) differs in its 5' UTR, including use of an alternate splice site compared to variant 1. This variant represents translation initiation at an alternate start codon compared to variant 1; the 5'-most initiation codon, as used in variant 1, is associated with a truncated ORF that would render the transcript a candidate for nonsense-mediated decay (NMD). Leaky scanning may allow translation initiation at the alternate start codon to encode an isoform (2) that has a shorter and distinct N-terminus, compared to isoform 1.
- Source sequence(s)
-
AI149177, BC105078, BE746724, BX399419
- UniProtKB/Swiss-Prot
-
Q0P5N6
- Related
-
ENST00000571082.5
-
NM_001329609.2 → NP_001316538.1 ADP-ribosylation factor-like protein 16 isoform 3
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) differs in the 5' UTR and lacks a portion of the 5' coding region, compared to variant 1. These differences cause translation initiation at a downstream start codon and result in an isoform (3) with a shorter N-terminus, compared to isoform 1.
- Source sequence(s)
-
AC139530, AI149177, BE746724, CN359525
- Consensus CDS
-
CCDS86652.1
- UniProtKB/TrEMBL
- I3L196, I3L1P0, I3L4Z7
- Related
- ENSP00000461674.1, ENST00000576135.5
- Conserved Domains (1) summary
-
- cl38936
Location:3 → 104
- P-loop_NTPase; P-loop containing Nucleoside Triphosphate Hydrolases
RNA
-
NR_138058.2 RNA Sequence
Status: REVIEWED
- Description
- Transcript Variant: This variant (4) contains an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AI149177, BC105078, BE746724, BG427716
-
NR_138059.1 RNA Sequence
Status: REVIEWED
- Source sequence(s)
-
AC139530, AI149177, BE746724, BF684514
- Related
-
ENST00000573392.5
-
NR_138060.1 RNA Sequence
Status: REVIEWED
- Source sequence(s)
-
AC139530, AI149177, BE746724, BG474883, DA088170
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
-
81681165..81683797 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060941.1 Alternate T2T-CHM13v2.0
- Range
-
82598066..82600691 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)