Canonical Allele Identifier: CA356792357

Gene: GRXCR1

Linked Data

• MyVariant Identifiers: chr4:g.42965038G>T (hg19) ; chr4:g.42963021G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42963021G>T , CM000666.2:g.42963021G>T	GRCh38
NC_000004.11:g.42965038G>T , CM000666.1:g.42965038G>T	GRCh37
NC_000004.10:g.42659795G>T	NCBI36
NG_027718.1:g.74756G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.514G>T MANE Select	ENSP00000382670.2:p.Glu172Ter
ENST00000399770.2:c.514G>T	ENSP00000382670.2:p.Glu172Ter
NM_001080476.2:c.514G>T	NP_001073945.1:p.Glu172Ter
XM_011513691.1:c.151G>T	XP_011511993.1:p.Glu51Ter
NM_001080476.3:c.514G>T MANE Select	NP_001073945.1:p.Glu172Ter