Canonical Allele Identifier: CA1964195797

Gene: RAG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36593759C= , CM000673.2:g.36593759C=	GRCh38
NC_000011.9:g.36615309C= , CM000673.1:g.36615309C=	GRCh37
NC_000011.8:g.36571885C=	NCBI36
NG_007573.1:g.9478G= , LRG_99:g.9478G=
NG_033154.1:g.4267C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527033.6:c.410G=	ENSP00000436895.2:p.Arg137=
ENST00000529083.2:c.410G=	ENSP00000436327.2:p.Arg137=
ENST00000532616.2:c.410G=	ENSP00000432174.2:p.Arg137=
ENST00000311485.8:c.410G= MANE Select	ENSP00000308620.4:p.Arg137=
ENST00000311485.7:c.410G=	ENSP00000308620.3:p.Arg137=
ENST00000524423.1:n.131+4343G=
ENST00000529083.1:c.410G=	ENSP00000436327.1:p.Arg137=
ENST00000618712.4:c.410G=	ENSP00000478672.1:p.Arg137=
NM_000536.3:c.410G=	NP_000527.2:p.Arg137=
NM_001243785.1:c.410G=	NP_001230714.1:p.Arg137=
NM_001243786.1:c.410G=	NP_001230715.1:p.Arg137=
NM_000536.4:c.410G= MANE Select	NP_000527.2:p.Arg137=
NM_001243785.2:c.410G=	NP_001230714.1:p.Arg137=
NM_001243786.2:c.410G=	NP_001230715.1:p.Arg137=