Canonical Allele Identifier: CA356792323

Gene: GRXCR1

Linked Data

• COSMIC: COSM4912724
• MyVariant Identifiers: chr4:g.42965023C>A (hg19) ; chr4:g.42963006C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42963006C>A , CM000666.2:g.42963006C>A	GRCh38
NC_000004.11:g.42965023C>A , CM000666.1:g.42965023C>A	GRCh37
NC_000004.10:g.42659780C>A	NCBI36
NG_027718.1:g.74741C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.499C>A MANE Select	ENSP00000382670.2:p.Arg167Ser
ENST00000399770.2:c.499C>A	ENSP00000382670.2:p.Arg167Ser
NM_001080476.2:c.499C>A	NP_001073945.1:p.Arg167Ser
XM_011513691.1:c.136C>A	XP_011511993.1:p.Arg46Ser
NM_001080476.3:c.499C>A MANE Select	NP_001073945.1:p.Arg167Ser