Canonical Allele Identifier: CA356792092

Gene: GRXCR1

Linked Data

• COSMIC: COSM1173058
• MyVariant Identifiers: chr4:g.42964908G>T (hg19) ; chr4:g.42962891G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42962891G>T , CM000666.2:g.42962891G>T	GRCh38
NC_000004.11:g.42964908G>T , CM000666.1:g.42964908G>T	GRCh37
NC_000004.10:g.42659665G>T	NCBI36
NG_027718.1:g.74626G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.385-1G>T MANE Select	ENSP00000382670.2:n.385-1G>T
ENST00000399770.2:c.385-1G>T	ENSP00000382670.2:n.385-1G>T
NM_001080476.2:c.385-1G>T	NP_001073945.1:n.385-1G>T
XM_011513691.1:c.22-1G>T	XP_011511993.1:n.22-1G>T
NM_001080476.3:c.385-1G>T MANE Select	NP_001073945.1:n.385-1G>T