Canonical Allele Identifier: CA356792162

Gene: GRXCR1

Linked Data

• MyVariant Identifiers: chr4:g.42964942G>T (hg19) ; chr4:g.42962925G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42962925G>T , CM000666.2:g.42962925G>T	GRCh38
NC_000004.11:g.42964942G>T , CM000666.1:g.42964942G>T	GRCh37
NC_000004.10:g.42659699G>T	NCBI36
NG_027718.1:g.74660G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.418G>T MANE Select	ENSP00000382670.2:p.Val140Leu
ENST00000399770.2:c.418G>T	ENSP00000382670.2:p.Val140Leu
NM_001080476.2:c.418G>T	NP_001073945.1:p.Val140Leu
XM_011513691.1:c.55G>T	XP_011511993.1:p.Val19Leu
NM_001080476.3:c.418G>T MANE Select	NP_001073945.1:p.Val140Leu