Canonical Allele Identifier: CA1453073800
Gene: GRXCR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963037T= , CM000666.2:g.42963037T= GRCh38
NC_000004.11:g.42965054T= , CM000666.1:g.42965054T= GRCh37
NC_000004.10:g.42659811T= NCBI36
NG_027718.1:g.74772T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.530T= MANE Select ENSP00000382670.2:p.Leu177=
ENST00000399770.2:c.530T= ENSP00000382670.2:p.Leu177=
NM_001080476.2:c.530T= NP_001073945.1:p.Leu177=
XM_011513691.1:c.167T= XP_011511993.1:p.Leu56=
NM_001080476.3:c.530T= MANE Select NP_001073945.1:p.Leu177=
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