Canonical Allele Identifier: CA1964192388

Gene: RAG2 RAG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36592604A= , CM000673.2:g.36592604A=	GRCh38
NC_000011.9:g.36614154A= , CM000673.1:g.36614154A=	GRCh37
NC_000011.8:g.36570730A=	NCBI36
NG_007573.1:g.10633T= , LRG_99:g.10633T=
NG_033154.1:g.3112A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527033.6:c.1565T= (RAG2)	ENSP00000436895.2:p.Leu522=
ENST00000529083.2:c.1565T= (RAG2)	ENSP00000436327.2:p.Leu522=
ENST00000532616.2:c.1565T= (RAG2)	ENSP00000432174.2:p.Leu522=
ENST00000311485.8:c.1565T= (RAG2) MANE Select	ENSP00000308620.4:p.Leu522=
ENST00000311485.7:c.1565T= (RAG2)	ENSP00000308620.3:p.Leu522=
ENST00000524423.1:n.131+5498T= (RAG2)
ENST00000534663.1:c.*86-363A= (RAG1)	ENSP00000434610.1:n.*86-363A=
ENST00000618712.4:c.1565T= (RAG2)	ENSP00000478672.1:p.Leu522=
NM_000536.3:c.1565T= (RAG2)	NP_000527.2:p.Leu522=
NM_001243785.1:c.1565T= (RAG2)	NP_001230714.1:p.Leu522=
NM_001243786.1:c.1565T= (RAG2)	NP_001230715.1:p.Leu522=
NM_000536.4:c.1565T= (RAG2) MANE Select	NP_000527.2:p.Leu522=
NM_001243785.2:c.1565T= (RAG2)	NP_001230714.1:p.Leu522=
NM_001243786.2:c.1565T= (RAG2)	NP_001230715.1:p.Leu522=