Canonical Allele Identifier: CA1453107700
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.43030547C= , CM000666.2:g.43030547C= GRCh38
NC_000004.11:g.43032564C= , CM000666.1:g.43032564C= GRCh37
NC_000004.10:g.42727321C= NCBI36
NG_027718.1:g.142282C=

Transcript Alleles

HGVS Amino-acid change
ENST00000399770.3:c.*7C= MANE Select ENSP00000382670.2:n.*7C=
ENST00000399770.2:c.880C= ENSP00000382670.2:n.880C=
NM_001080476.2:c.*7C= NP_001073945.1:n.*7C=
XM_011513691.1:c.*7C= XP_011511993.1:n.*7C=
NM_001080476.3:c.*7C= MANE Select NP_001073945.1:n.*7C=