Canonical Allele Identifier: CA380142669

Gene: RAG2

Linked Data

• MyVariant Identifiers: chr11:g.36615192G>A (hg19) ; chr11:g.36593642G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36593642G>A , CM000673.2:g.36593642G>A	GRCh38
NC_000011.9:g.36615192G>A , CM000673.1:g.36615192G>A	GRCh37
NC_000011.8:g.36571768G>A	NCBI36
NG_007573.1:g.9595C>T , LRG_99:g.9595C>T
NG_033154.1:g.4150G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527033.6:c.527C>T	ENSP00000436895.2:p.Ala176Val
ENST00000529083.2:c.527C>T	ENSP00000436327.2:p.Ala176Val
ENST00000532616.2:c.527C>T	ENSP00000432174.2:p.Ala176Val
ENST00000311485.8:c.527C>T MANE Select	ENSP00000308620.4:p.Ala176Val
ENST00000311485.7:c.527C>T	ENSP00000308620.3:p.Ala176Val
ENST00000524423.1:n.131+4460C>T
ENST00000618712.4:c.527C>T	ENSP00000478672.1:p.Ala176Val
NM_000536.3:c.527C>T	NP_000527.2:p.Ala176Val
NM_001243785.1:c.527C>T	NP_001230714.1:p.Ala176Val
NM_001243786.1:c.527C>T	NP_001230715.1:p.Ala176Val
NM_000536.4:c.527C>T MANE Select	NP_000527.2:p.Ala176Val
NM_001243785.2:c.527C>T	NP_001230714.1:p.Ala176Val
NM_001243786.2:c.527C>T	NP_001230715.1:p.Ala176Val