Canonical Allele Identifier: CA356792334
Gene: GRXCR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963012A>G , CM000666.2:g.42963012A>G GRCh38
NC_000004.11:g.42965029A>G , CM000666.1:g.42965029A>G GRCh37
NC_000004.10:g.42659786A>G NCBI36
NG_027718.1:g.74747A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.505A>G MANE Select ENSP00000382670.2:p.Lys169Glu
ENST00000399770.2:c.505A>G ENSP00000382670.2:p.Lys169Glu
NM_001080476.2:c.505A>G NP_001073945.1:p.Lys169Glu
XM_011513691.1:c.142A>G XP_011511993.1:p.Lys48Glu
NM_001080476.3:c.505A>G MANE Select NP_001073945.1:p.Lys169Glu