Canonical Allele Identifier: CA1453073766
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962971G= , CM000666.2:g.42962971G= GRCh38
NC_000004.11:g.42964988G= , CM000666.1:g.42964988G= GRCh37
NC_000004.10:g.42659745G= NCBI36
NG_027718.1:g.74706G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.464G= MANE Select ENSP00000382670.2:p.Arg155=
ENST00000399770.2:c.464G= ENSP00000382670.2:p.Arg155=
NM_001080476.2:c.464G= NP_001073945.1:p.Arg155=
XM_011513691.1:c.101G= XP_011511993.1:p.Arg34=
NM_001080476.3:c.464G= MANE Select NP_001073945.1:p.Arg155=