Canonical Allele Identifier: CA1453073880

Gene: GRXCR1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42963176C= , CM000666.2:g.42963176C=	GRCh38
NC_000004.11:g.42965193C= , CM000666.1:g.42965193C=	GRCh37
NC_000004.10:g.42659950C=	NCBI36
NG_027718.1:g.74911C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.627+42C= MANE Select	ENSP00000382670.2:n.627+42C=
ENST00000399770.2:c.627+42C=	ENSP00000382670.2:n.627+42C=
NM_001080476.2:c.627+42C=	NP_001073945.1:n.627+42C=
XM_011513691.1:c.264+42C=	XP_011511993.1:n.264+42C=
NM_001080476.3:c.627+42C= MANE Select	NP_001073945.1:n.627+42C=