Canonical Allele Identifier: CA1964196705

Gene: RAG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36594065C= , CM000673.2:g.36594065C=	GRCh38
NC_000011.9:g.36615615C= , CM000673.1:g.36615615C=	GRCh37
NC_000011.8:g.36572191C=	NCBI36
NG_007573.1:g.9172G= , LRG_99:g.9172G=
NG_033154.1:g.4573C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000536.4:c.104G= MANE Select	NP_000527.2:p.Gly35=
ENST00000311485.8:c.104G= MANE Select	ENSP00000308620.4:p.Gly35=
NM_000536.3:c.104G=	NP_000527.2:p.Gly35=
NM_001243785.1:c.104G=	NP_001230714.1:p.Gly35=
NM_001243785.2:c.104G=	NP_001230714.1:p.Gly35=
NM_001243786.1:c.104G=	NP_001230715.1:p.Gly35=
NM_001243786.2:c.104G=	NP_001230715.1:p.Gly35=
ENST00000311485.7:c.104G=	ENSP00000308620.3:p.Gly35=
ENST00000524423.1:n.131+4037G=
ENST00000527033.5:c.104G=	ENSP00000436895.1:p.Gly35=
ENST00000527033.6:c.104G=	ENSP00000436895.2:p.Gly35=
ENST00000529083.1:c.104G=	ENSP00000436327.1:p.Gly35=
ENST00000529083.2:c.104G=	ENSP00000436327.2:p.Gly35=
ENST00000532616.2:c.104G=	ENSP00000432174.2:p.Gly35=
ENST00000618712.4:c.104G=	ENSP00000478672.1:p.Gly35=