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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_032119.1 RefSeqGene
- Range
-
5001..85628
- Download
- GenBank, FASTA, Sequence Viewer (Graphics), LRG_424
mRNA and Protein(s)
-
NM_000677.4 → NP_000668.1 adenosine receptor A3 isoform A
See identical proteins and their annotated locations for NP_000668.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (A) encodes the longest isoform (A).
- Source sequence(s)
-
AL390195
- Consensus CDS
-
CCDS839.1
- UniProtKB/Swiss-Prot
- A2A3P4, P0DMS8, P33765, Q6UWU0, Q9BYZ1
- UniProtKB/TrEMBL
- B2R7S2, H6VQ59
- Related
- ENSP00000241356.4, ENST00000241356.5
- Conserved Domains (2) summary
-
- cd14964
Location:15 → 39
- 7tm_GPCRs; TM helix 1 [structural motif]
- cl28897
Location:13 → 293
- 7tm_GPCRs; seven-transmembrane G protein-coupled receptor superfamily
-
NM_001302678.2 → NP_001289607.1 adenosine receptor A3 isoform B
Status: REVIEWED
- Description
- Transcript Variant: This variant (B) uses an alternate splice site in the 3' terminal exon, resulting in an alternate 3' coding region and 3' UTR, compared to variant A. The encoded isoform (B) has a distinct C-terminus and is shorter than isoform A.
- Source sequence(s)
-
AL390195, BF432324, BM675096, CD013875, JN855714
- Consensus CDS
-
CCDS81358.1
- UniProtKB/TrEMBL
-
A0A0J9YWR0
- Related
- ENSP00000488073.1, ENST00000632535.1
- Conserved Domains (2) summary
-
- cd14964
Location:14 → 40
- 7tm_GPCRs; TM helix 1 [structural motif]
- cl28897
Location:13 → 116
- 7tm_GPCRs; seven-transmembrane G protein-coupled receptor superfamily
-
NM_001302679.2 → NP_001289608.1 adenosine receptor A3 isoform C
Status: REVIEWED
- Description
- Transcript Variant: This variant (C) uses an alternate splice site in the 5' terminal exon, and it thus differs in its 5' UTR, lacks a portion of the 5' coding region, and initiates translation at a downstream in-frame start codon, compared to variant A. The encoded isoform (C) is shorter at the N-terminus, compared to isoform A.
- Source sequence(s)
-
AL390195, BF432324, BM675096, BX283401, JN855714
- UniProtKB/TrEMBL
-
H6VQ59
- Conserved Domains (2) summary
-
- cd14964
Location:29 → 59
- 7tm_GPCRs; TM helix 5 [structural motif]
- cl28897
Location:1 → 148
- 7tm_GPCRs; seven-transmembrane G protein-coupled receptor superfamily
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_000001.11 Reference GRCh38.p14 Primary Assembly
- Range
-
111499429..111503633 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060925.1 Alternate T2T-CHM13v2.0
- Range
-
111514110..111518318 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)