Canonical Allele Identifier: CA1964169595

Gene: RAG1 RAG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36576455A= , CM000673.2:g.36576455A=	GRCh38
NC_000011.9:g.36598005A= , CM000673.1:g.36598005A=	GRCh37
NC_000011.8:g.36554581A=	NCBI36
NG_007528.1:g.13443A= , LRG_98:g.13443A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697713.1:c.*19A= (RAG1)	ENSP00000513411.1:n.*19A=
ENST00000697714.1:c.*19A= (RAG1)	ENSP00000513412.1:n.*19A=
ENST00000697715.1:c.*19A= (RAG1)	ENSP00000513413.1:n.*19A=
ENST00000299440.6:c.*19A= (RAG1) MANE Select	ENSP00000299440.5:n.*19A=
ENST00000299440.5:c.*19A= (RAG1)	ENSP00000299440.5:n.*19A=
ENST00000524423.1:n.132-484T= (RAG2)
ENST00000534663.1:c.2789+362A= (RAG1)	ENSP00000434610.1:n.2789+362A=
NM_000448.2:c.*19A= , LRG_98t1:c.*19A= (RAG1)	NP_000439.1:n.*19A=
XM_005253041.3:c.*19A= (RAG1)	XP_005253098.1:n.*19A=
XM_011520250.1:c.*19A= (RAG1)	XP_011518552.1:n.*19A=
XM_011520251.1:c.*19A= (RAG1)	XP_011518553.1:n.*19A=
XM_005253041.4:c.*19A= (RAG1)	XP_005253098.1:n.*19A=
XM_011520250.2:c.*19A= (RAG1)	XP_011518552.1:n.*19A=
NM_000448.3:c.*19A= (RAG1) MANE Select	NP_000439.2:n.*19A=
NM_001377277.1:c.*19A= (RAG1)	NP_001364206.1:n.*19A=
NM_001377278.1:c.*19A= (RAG1)	NP_001364207.1:n.*19A=
NM_001377279.1:c.*19A= (RAG1)	NP_001364208.1:n.*19A=
NM_001377280.1:c.*19A= (RAG1)	NP_001364209.1:n.*19A=