Linked Data
ClinVar Variation Id:
13145
ClinVar RCV Id:
RCV000014027
dbSNP Id:
rs104894290
PubMed:
PMID:9630231
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.36576039A>G , CM000673.2:g.36576039A>G | GRCh38 |
| NC_000011.9:g.36597589A>G , CM000673.1:g.36597589A>G | GRCh37 |
| NC_000011.8:g.36554165A>G | NCBI36 |
| NG_007528.1:g.13027A>G , LRG_98:g.13027A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000697713.1:c.2735A>G (RAG1) | ENSP00000513411.1:p.Tyr912Cys | |
| ENST00000697714.1:c.2735A>G (RAG1) | ENSP00000513412.1:p.Tyr912Cys | |
| ENST00000697715.1:c.2735A>G (RAG1) | ENSP00000513413.1:p.Tyr912Cys | |
| ENST00000299440.6:c.2735A>G (RAG1) MANE Select | ENSP00000299440.5:p.Tyr912Cys | |
| ENST00000299440.5:c.2735A>G (RAG1) | ENSP00000299440.5:p.Tyr912Cys | |
| ENST00000524423.1:n.132-68T>C (RAG2) | ||
| ENST00000534663.1:c.2735A>G (RAG1) | ENSP00000434610.1:p.Tyr912Cys | |
| NM_000448.2:c.2735A>G , LRG_98t1:c.2735A>G (RAG1) | NP_000439.1:p.Tyr912Cys | |
| XM_005253041.3:c.2735A>G (RAG1) | XP_005253098.1:p.Tyr912Cys | |
| XM_011520250.1:c.2735A>G (RAG1) | XP_011518552.1:p.Tyr912Cys | |
| XM_011520251.1:c.2735A>G (RAG1) | XP_011518553.1:p.Tyr912Cys | |
| XM_005253041.4:c.2735A>G (RAG1) | XP_005253098.1:p.Tyr912Cys | |
| XM_011520250.2:c.2735A>G (RAG1) | XP_011518552.1:p.Tyr912Cys | |
| NM_000448.3:c.2735A>G (RAG1) MANE Select | NP_000439.2:p.Tyr912Cys | |
| NM_001377277.1:c.2735A>G (RAG1) | NP_001364206.1:p.Tyr912Cys | |
| NM_001377278.1:c.2735A>G (RAG1) | NP_001364207.1:p.Tyr912Cys | |
| NM_001377279.1:c.2735A>G (RAG1) | NP_001364208.1:p.Tyr912Cys | |
| NM_001377280.1:c.2735A>G (RAG1) | NP_001364209.1:p.Tyr912Cys |