Canonical Allele Identifier: CA13379507

Gene: RAG1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36512203G>A , CM000673.2:g.36512203G>A	GRCh38
NC_000011.9:g.36533753G>A , CM000673.1:g.36533753G>A	GRCh37
NC_000011.8:g.36490329G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697713.1:c.-131+1666G>A	ENSP00000513411.1:n.-131+1666G>A
ENST00000697714.1:c.-15+1666G>A	ENSP00000513412.1:n.-15+1666G>A
ENST00000697715.1:c.-289+1666G>A	ENSP00000513413.1:n.-289+1666G>A
ENST00000529126.5:n.330+1165G>A
XM_005253041.3:c.-15+1666G>A	XP_005253098.1:n.-15+1666G>A
XM_011520250.1:c.-129+1666G>A	XP_011518552.1:n.-129+1666G>A
XM_011520251.1:c.-227+1666G>A	XP_011518553.1:n.-227+1666G>A
XM_005253041.4:c.-15+1666G>A	XP_005253098.1:n.-15+1666G>A
XM_011520250.2:c.-129+1666G>A	XP_011518552.1:n.-129+1666G>A
NM_001377277.1:c.-289+1666G>A	NP_001364206.1:n.-289+1666G>A
NM_001377278.1:c.-227+1666G>A	NP_001364207.1:n.-227+1666G>A
NM_001377279.1:c.-129+1666G>A	NP_001364208.1:n.-129+1666G>A
NM_001377280.1:c.-15+1666G>A	NP_001364209.1:n.-15+1666G>A