Canonical Allele Identifier: CA2000617596
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228568_112228571delinsTGAC , CM000673.2:g.112228568_112228571delinsTGAC GRCh38
NC_000011.9:g.112099291_112099294delinsTGAC , CM000673.1:g.112099291_112099294delinsTGAC GRCh37
NC_000011.8:g.111604501_111604504delinsTGAC NCBI36
NG_008743.1:g.7204_7207delinsTGAC

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.84-26_84-23delinsTGAC MANE Select ENSP00000280362.3:n.84-26_84-23delinsTGAC...
ENST00000280362.7:c.84-26_84-23delinsTGAC ENSP00000280362.3:n.84-26_84-23delinsTGAC...
ENST00000524931.1:c.-121-26_-121-23delinsTGAC ENSP00000434688.1:n.-121-26_-121-23delins...
ENST00000525645.1:n.159-26_159-23delinsTGAC
ENST00000525803.1:c.84-26_84-23delinsTGAC ENSP00000431750.1:n.84-26_84-23delinsTGAC...
ENST00000528679.5:c.84-26_84-23delinsTGAC ENSP00000435895.1:n.84-26_84-23delinsTGAC...
ENST00000531673.5:c.84-26_84-23delinsTGAC ENSP00000433469.1:n.84-26_84-23delinsTGAC...
NM_000317.2:c.84-26_84-23delinsTGAC NP_000308.1:n.84-26_84-23delinsTGAC
NM_000317.3:c.84-26_84-23delinsTGAC MANE Select NP_000308.1:n.84-26_84-23delinsTGAC