Canonical Allele Identifier: CA1453107613
Community Standard Title: NM_001080476.3(GRXCR1):c.694-5T=
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.43030356T= , CM000666.2:g.43030356T= GRCh38
NC_000004.11:g.43032373T= , CM000666.1:g.43032373T= GRCh37
NC_000004.10:g.42727130T= NCBI36
NG_027718.1:g.142091T=

Transcript Alleles

HGVS Amino-acid Change
NM_001080476.3:c.694-5T= MANE Select NP_001073945.1:n.694-5T=
ENST00000399770.3:c.694-5T= MANE Select ENSP00000382670.2:n.694-5T=
NM_001080476.2:c.694-5T= NP_001073945.1:n.694-5T=
ENST00000399770.2:c.694-5T= ENSP00000382670.2:n.694-5T=
XM_011513691.1:c.331-5T= XP_011511993.1:n.331-5T=