Canonical Allele Identifier: CA1453073735
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962905A= , CM000666.2:g.42962905A= GRCh38
NC_000004.11:g.42964922A= , CM000666.1:g.42964922A= GRCh37
NC_000004.10:g.42659679A= NCBI36
NG_027718.1:g.74640A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.398A= MANE Select ENSP00000382670.2:p.Asp133=
ENST00000399770.2:c.398A= ENSP00000382670.2:p.Asp133=
NM_001080476.2:c.398A= NP_001073945.1:p.Asp133=
XM_011513691.1:c.35A= XP_011511993.1:p.Asp12=
NM_001080476.3:c.398A= MANE Select NP_001073945.1:p.Asp133=