Canonical Allele Identifier: CA2695215385
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228595_112228606del , CM000673.2:g.112228595_112228606del GRCh38
NC_000011.9:g.112099318_112099329del , CM000673.1:g.112099318_112099329del GRCh37
NC_000011.8:g.111604528_111604539del NCBI36
NG_008743.1:g.7231_7242del

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.8:c.85_96del
ENST00000280362.7:c.85_96del
ENST00000524931.1:c.-120_-109del
ENST00000525645.1:n.160_171del
ENST00000525803.1:c.85_96del
ENST00000528679.5:c.85_96del
ENST00000531673.5:c.85_96del
NM_000317.2:c.85_96del
NM_000317.3:c.85_96del