Canonical Allele Identifier: CA1453073754
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962949G= , CM000666.2:g.42962949G= GRCh38
NC_000004.11:g.42964966G= , CM000666.1:g.42964966G= GRCh37
NC_000004.10:g.42659723G= NCBI36
NG_027718.1:g.74684G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.442G= MANE Select ENSP00000382670.2:p.Val148=
ENST00000399770.2:c.442G= ENSP00000382670.2:p.Val148=
NM_001080476.2:c.442G= NP_001073945.1:p.Val148=
XM_011513691.1:c.79G= XP_011511993.1:p.Val27=
NM_001080476.3:c.442G= MANE Select NP_001073945.1:p.Val148=