Canonical Allele Identifier: CA1453107694
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.43030535G= , CM000666.2:g.43030535G= GRCh38
NC_000004.11:g.43032552G= , CM000666.1:g.43032552G= GRCh37
NC_000004.10:g.42727309G= NCBI36
NG_027718.1:g.142270G=

Transcript Alleles

HGVS Amino-acid change
ENST00000399770.3:c.868G= MANE Select ENSP00000382670.2:p.Gly290=
ENST00000399770.2:c.868G= ENSP00000382670.2:p.Gly290=
NM_001080476.2:c.868G= NP_001073945.1:p.Gly290=
XM_011513691.1:c.505G= XP_011511993.1:p.Gly169=
NM_001080476.3:c.868G= MANE Select NP_001073945.1:p.Gly290=