Canonical Allele Identifier: CA380153552

Gene: RAG1

Linked Data

• dbSNP Id: rs1322150766
• gnomAD v2: 11-36596757-G-A
• gnomAD v4: 11-36575207-G-A
• MyVariant Identifiers: chr11:g.36596757G>A (hg19) ; chr11:g.36575207G>A (hg38)

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