Canonical Allele Identifier: CA380153552
Gene: RAG1 HGNC NCBI

Linked Data

dbSNP Id: rs1322150766

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36575207G>A , CM000673.2:g.36575207G>A GRCh38
NC_000011.9:g.36596757G>A , CM000673.1:g.36596757G>A GRCh37
NC_000011.8:g.36553333G>A NCBI36
NG_007528.1:g.12195G>A , LRG_98:g.12195G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697713.1:c.1903G>A ENSP00000513411.1:p.Ala635Thr
ENST00000697714.1:c.1903G>A ENSP00000513412.1:p.Ala635Thr
ENST00000697715.1:c.1903G>A ENSP00000513413.1:p.Ala635Thr
ENST00000299440.6:c.1903G>A MANE Select ENSP00000299440.5:p.Ala635Thr
ENST00000299440.5:c.1903G>A ENSP00000299440.5:p.Ala635Thr
ENST00000534663.1:c.1903G>A ENSP00000434610.1:p.Ala635Thr
NM_000448.2:c.1903G>A , LRG_98t1:c.1903G>A NP_000439.1:p.Ala635Thr
XM_005253041.3:c.1903G>A XP_005253098.1:p.Ala635Thr
XM_011520250.1:c.1903G>A XP_011518552.1:p.Ala635Thr
XM_011520251.1:c.1903G>A XP_011518553.1:p.Ala635Thr
XM_005253041.4:c.1903G>A XP_005253098.1:p.Ala635Thr
XM_011520250.2:c.1903G>A XP_011518552.1:p.Ala635Thr
NM_000448.3:c.1903G>A MANE Select NP_000439.2:p.Ala635Thr
NM_001377277.1:c.1903G>A NP_001364206.1:p.Ala635Thr
NM_001377278.1:c.1903G>A NP_001364207.1:p.Ala635Thr
NM_001377279.1:c.1903G>A NP_001364208.1:p.Ala635Thr
NM_001377280.1:c.1903G>A NP_001364209.1:p.Ala635Thr