Canonical Allele Identifier: CA1964169599

Gene: RAG1 RAG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36576457T= , CM000673.2:g.36576457T=	GRCh38
NC_000011.9:g.36598007T= , CM000673.1:g.36598007T=	GRCh37
NC_000011.8:g.36554583T=	NCBI36
NG_007528.1:g.13445T= , LRG_98:g.13445T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697713.1:c.*21T= (RAG1)	ENSP00000513411.1:n.*21T=
ENST00000697714.1:c.*21T= (RAG1)	ENSP00000513412.1:n.*21T=
ENST00000697715.1:c.*21T= (RAG1)	ENSP00000513413.1:n.*21T=
ENST00000299440.6:c.*21T= (RAG1) MANE Select	ENSP00000299440.5:n.*21T=
ENST00000299440.5:c.*21T= (RAG1)	ENSP00000299440.5:n.*21T=
ENST00000524423.1:n.132-486A= (RAG2)
ENST00000534663.1:c.2789+364T= (RAG1)	ENSP00000434610.1:n.2789+364T=
NM_000448.2:c.*21T= , LRG_98t1:c.*21T= (RAG1)	NP_000439.1:n.*21T=
XM_005253041.3:c.*21T= (RAG1)	XP_005253098.1:n.*21T=
XM_011520250.1:c.*21T= (RAG1)	XP_011518552.1:n.*21T=
XM_011520251.1:c.*21T= (RAG1)	XP_011518553.1:n.*21T=
XM_005253041.4:c.*21T= (RAG1)	XP_005253098.1:n.*21T=
XM_011520250.2:c.*21T= (RAG1)	XP_011518552.1:n.*21T=
NM_000448.3:c.*21T= (RAG1) MANE Select	NP_000439.2:n.*21T=
NM_001377277.1:c.*21T= (RAG1)	NP_001364206.1:n.*21T=
NM_001377278.1:c.*21T= (RAG1)	NP_001364207.1:n.*21T=
NM_001377279.1:c.*21T= (RAG1)	NP_001364208.1:n.*21T=
NM_001377280.1:c.*21T= (RAG1)	NP_001364209.1:n.*21T=