Canonical Allele Identifier: CA942298761
Gene: PTS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228607_112228613del , CM000673.2:g.112228607_112228613del GRCh38
NC_000011.9:g.112099330_112099336del , CM000673.1:g.112099330_112099336del GRCh37
NC_000011.8:g.111604540_111604546del NCBI36
NG_008743.1:g.7243_7249del

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.8:c.97_103del MANE Select ENSP00000280362.3:p.Asp33LysfsTer3
ENST00000280362.7:c.97_103del ENSP00000280362.3:p.Asp33LysfsTer3
ENST00000524931.1:c.-108_-102del ENSP00000434688.1:n.-108_-102del
ENST00000525645.1:n.172_178del
ENST00000525803.1:c.97_103del ENSP00000431750.1:p.Asp33LysfsTer3
ENST00000528679.5:c.97_103del ENSP00000435895.1:p.Asp33LysfsTer3
ENST00000531673.5:c.97_103del ENSP00000433469.1:p.Asp33LysfsTer3
NM_000317.2:c.97_103del NP_000308.1:p.Asp33LysfsTer3
NM_000317.3:c.97_103del MANE Select NP_000308.1:p.Asp33LysfsTer3
Search 100 bp 5'
Search 100 bp 3'