Canonical Allele Identifier: CA1964196681

Gene: RAG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36594054T= , CM000673.2:g.36594054T=	GRCh38
NC_000011.9:g.36615604T= , CM000673.1:g.36615604T=	GRCh37
NC_000011.8:g.36572180T=	NCBI36
NG_007573.1:g.9183A= , LRG_99:g.9183A=
NG_033154.1:g.4562T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000527033.6:c.115A=	ENSP00000436895.2:p.Arg39=
ENST00000529083.2:c.115A=	ENSP00000436327.2:p.Arg39=
ENST00000532616.2:c.115A=	ENSP00000432174.2:p.Arg39=
ENST00000311485.8:c.115A= MANE Select	ENSP00000308620.4:p.Arg39=
ENST00000311485.7:c.115A=	ENSP00000308620.3:p.Arg39=
ENST00000524423.1:n.131+4048A=
ENST00000527033.5:c.115A=	ENSP00000436895.1:p.Arg39=
ENST00000529083.1:c.115A=	ENSP00000436327.1:p.Arg39=
ENST00000618712.4:c.115A=	ENSP00000478672.1:p.Arg39=
NM_000536.3:c.115A=	NP_000527.2:p.Arg39=
NM_001243785.1:c.115A=	NP_001230714.1:p.Arg39=
NM_001243786.1:c.115A=	NP_001230715.1:p.Arg39=
NM_000536.4:c.115A= MANE Select	NP_000527.2:p.Arg39=
NM_001243785.2:c.115A=	NP_001230714.1:p.Arg39=
NM_001243786.2:c.115A=	NP_001230715.1:p.Arg39=