Canonical Allele Identifier: CA1453073726
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962892C= , CM000666.2:g.42962892C= GRCh38
NC_000004.11:g.42964909C= , CM000666.1:g.42964909C= GRCh37
NC_000004.10:g.42659666C= NCBI36
NG_027718.1:g.74627C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.385C= MANE Select ENSP00000382670.2:p.Gln129=
ENST00000399770.2:c.385C= ENSP00000382670.2:p.Gln129=
NM_001080476.2:c.385C= NP_001073945.1:p.Gln129=
XM_011513691.1:c.22C= XP_011511993.1:p.Gln8=
NM_001080476.3:c.385C= MANE Select NP_001073945.1:p.Gln129=