Canonical Allele Identifier: CA474031596

Gene: RAG1

Linked Data

• MyVariant Identifiers: chr11:g.36595823C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36574273C>T , CM000673.2:g.36574273C>T	GRCh38
NC_000011.9:g.36595823C>T , CM000673.1:g.36595823C>T	GRCh37
NC_000011.8:g.36552399C>T	NCBI36
NG_007528.1:g.11261C>T , LRG_98:g.11261C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697713.1:c.969C>T	ENSP00000513411.1:p.Val323=
ENST00000697714.1:c.969C>T	ENSP00000513412.1:p.Val323=
ENST00000697715.1:c.969C>T	ENSP00000513413.1:p.Val323=
ENST00000299440.6:c.969C>T MANE Select	ENSP00000299440.5:p.Val323=
ENST00000299440.5:c.969C>T	ENSP00000299440.5:p.Val323=
ENST00000534663.1:c.969C>T	ENSP00000434610.1:p.Val323=
NM_000448.2:c.969C>T , LRG_98t1:c.969C>T	NP_000439.1:p.Val323=
XM_005253041.3:c.969C>T	XP_005253098.1:p.Val323=
XM_011520250.1:c.969C>T	XP_011518552.1:p.Val323=
XM_011520251.1:c.969C>T	XP_011518553.1:p.Val323=
XM_005253041.4:c.969C>T	XP_005253098.1:p.Val323=
XM_011520250.2:c.969C>T	XP_011518552.1:p.Val323=
NM_000448.3:c.969C>T MANE Select	NP_000439.2:p.Val323=
NM_001377277.1:c.969C>T	NP_001364206.1:p.Val323=
NM_001377278.1:c.969C>T	NP_001364207.1:p.Val323=
NM_001377279.1:c.969C>T	NP_001364208.1:p.Val323=
NM_001377280.1:c.969C>T	NP_001364209.1:p.Val323=