Canonical Allele Identifier: CA375280523
Community Standard Title: NM_032728.4(PLPP7):c.179G>A (p.Arg60His)
Gene: PLPP7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131290176G>A , CM000671.2:g.131290176G>A GRCh38
NC_000009.11:g.134165563G>A , CM000671.1:g.134165563G>A GRCh37
NC_000009.10:g.133155384G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_032728.4:c.179G>A MANE Select NP_116117.3:p.Arg60His
ENST00000372264.4:c.179G>A MANE Select ENSP00000361338.3:p.Arg60His
NM_032728.3:c.179G>A NP_116117.3:p.Arg60His
ENST00000372261.1:c.179G>A ENSP00000361335.1:p.Arg60His
ENST00000372264.3:c.179G>A ENSP00000361338.3:p.Arg60His
ENST00000645295.1:c.179G>A ENSP00000494088.1:p.Arg60His
XM_005272230.2:c.179G>A XP_005272287.1:p.Arg60His
XM_005272230.4:c.179G>A XP_005272287.1:p.Arg60His
XM_005272231.1:c.179G>A XP_005272288.1:p.Arg60His
XM_005272231.2:c.179G>A XP_005272288.1:p.Arg60His