Canonical Allele Identifier: CA1453073732
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962899C= , CM000666.2:g.42962899C= GRCh38
NC_000004.11:g.42964916C= , CM000666.1:g.42964916C= GRCh37
NC_000004.10:g.42659673C= NCBI36
NG_027718.1:g.74634C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.392C= MANE Select ENSP00000382670.2:p.Ser131=
ENST00000399770.2:c.392C= ENSP00000382670.2:p.Ser131=
NM_001080476.2:c.392C= NP_001073945.1:p.Ser131=
XM_011513691.1:c.29C= XP_011511993.1:p.Ser10=
NM_001080476.3:c.392C= MANE Select NP_001073945.1:p.Ser131=