Canonical Allele Identifier: CA1453073696
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962823T= , CM000666.2:g.42962823T= GRCh38
NC_000004.11:g.42964840T= , CM000666.1:g.42964840T= GRCh37
NC_000004.10:g.42659597T= NCBI36
NG_027718.1:g.74558T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.385-69T= MANE Select ENSP00000382670.2:n.385-69T=
ENST00000399770.2:c.385-69T= ENSP00000382670.2:n.385-69T=
NM_001080476.2:c.385-69T= NP_001073945.1:n.385-69T=
XM_011513691.1:c.22-69T= XP_011511993.1:n.22-69T=
NM_001080476.3:c.385-69T= MANE Select NP_001073945.1:n.385-69T=