Canonical Allele Identifier: CA1453073723
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962885C= , CM000666.2:g.42962885C= GRCh38
NC_000004.11:g.42964902C= , CM000666.1:g.42964902C= GRCh37
NC_000004.10:g.42659659C= NCBI36
NG_027718.1:g.74620C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.385-7C= MANE Select ENSP00000382670.2:n.385-7C=
ENST00000399770.2:c.385-7C= ENSP00000382670.2:n.385-7C=
NM_001080476.2:c.385-7C= NP_001073945.1:n.385-7C=
XM_011513691.1:c.22-7C= XP_011511993.1:n.22-7C=
NM_001080476.3:c.385-7C= MANE Select NP_001073945.1:n.385-7C=