Canonical Allele Identifier: CA1964193060

Gene: RAG2 RAG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36592837G= , CM000673.2:g.36592837G=	GRCh38
NC_000011.9:g.36614387G= , CM000673.1:g.36614387G=	GRCh37
NC_000011.8:g.36570963G=	NCBI36
NG_007573.1:g.10400C= , LRG_99:g.10400C=
NG_033154.1:g.3345G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527033.6:c.1332C= (RAG2)	ENSP00000436895.2:p.Ile444=
ENST00000529083.2:c.1332C= (RAG2)	ENSP00000436327.2:p.Ile444=
ENST00000532616.2:c.1332C= (RAG2)	ENSP00000432174.2:p.Ile444=
ENST00000311485.8:c.1332C= (RAG2) MANE Select	ENSP00000308620.4:p.Ile444=
ENST00000311485.7:c.1332C= (RAG2)	ENSP00000308620.3:p.Ile444=
ENST00000524423.1:n.131+5265C= (RAG2)
ENST00000534663.1:c.*86-130G= (RAG1)	ENSP00000434610.1:n.*86-130G=
ENST00000618712.4:c.1332C= (RAG2)	ENSP00000478672.1:p.Ile444=
NM_000536.3:c.1332C= (RAG2)	NP_000527.2:p.Ile444=
NM_001243785.1:c.1332C= (RAG2)	NP_001230714.1:p.Ile444=
NM_001243786.1:c.1332C= (RAG2)	NP_001230715.1:p.Ile444=
NM_000536.4:c.1332C= (RAG2) MANE Select	NP_000527.2:p.Ile444=
NM_001243785.2:c.1332C= (RAG2)	NP_001230714.1:p.Ile444=
NM_001243786.2:c.1332C= (RAG2)	NP_001230715.1:p.Ile444=