Canonical Allele Identifier: CA356792335

Gene: GRXCR1

Linked Data

• COSMIC: COSM1253849
• MyVariant Identifiers: chr4:g.42965030A>C (hg19) ; chr4:g.42963013A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42963013A>C , CM000666.2:g.42963013A>C	GRCh38
NC_000004.11:g.42965030A>C , CM000666.1:g.42965030A>C	GRCh37
NC_000004.10:g.42659787A>C	NCBI36
NG_027718.1:g.74748A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.506A>C MANE Select	ENSP00000382670.2:p.Lys169Thr
ENST00000399770.2:c.506A>C	ENSP00000382670.2:p.Lys169Thr
NM_001080476.2:c.506A>C	NP_001073945.1:p.Lys169Thr
XM_011513691.1:c.143A>C	XP_011511993.1:p.Lys48Thr
NM_001080476.3:c.506A>C MANE Select	NP_001073945.1:p.Lys169Thr