Canonical Allele Identifier: CA1453073761

Gene: GRXCR1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42962959C= , CM000666.2:g.42962959C=	GRCh38
NC_000004.11:g.42964976C= , CM000666.1:g.42964976C=	GRCh37
NC_000004.10:g.42659733C=	NCBI36
NG_027718.1:g.74694C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.452C= MANE Select	ENSP00000382670.2:p.Thr151=
ENST00000399770.2:c.452C=	ENSP00000382670.2:p.Thr151=
NM_001080476.2:c.452C=	NP_001073945.1:p.Thr151=
XM_011513691.1:c.89C=	XP_011511993.1:p.Thr30=
NM_001080476.3:c.452C= MANE Select	NP_001073945.1:p.Thr151=