Canonical Allele Identifier: CA2000617569
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228515_112228519delinsTAATA , CM000673.2:g.112228515_112228519delinsTAATA GRCh38
NC_000011.9:g.112099238_112099242delinsTAATA , CM000673.1:g.112099238_112099242delinsTAATA GRCh37
NC_000011.8:g.111604448_111604452delinsTAATA NCBI36
NG_008743.1:g.7151_7155delinsTAATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.8:c.84-79_84-75delinsTAATA MANE Select ENSP00000280362.3:n.84-79_84-75delinsTAATA
ENST00000280362.7:c.84-79_84-75delinsTAATA ENSP00000280362.3:n.84-79_84-75delinsTAATA
ENST00000524931.1:c.-121-79_-121-75delinsTAATA ENSP00000434688.1:n.-121-79_-121-75delinsTAATA
ENST00000525645.1:n.159-79_159-75delinsTAATA
ENST00000525803.1:c.84-79_84-75delinsTAATA ENSP00000431750.1:n.84-79_84-75delinsTAATA
ENST00000528679.5:c.84-79_84-75delinsTAATA ENSP00000435895.1:n.84-79_84-75delinsTAATA
ENST00000531673.5:c.84-79_84-75delinsTAATA ENSP00000433469.1:n.84-79_84-75delinsTAATA
NM_000317.2:c.84-79_84-75delinsTAATA NP_000308.1:n.84-79_84-75delinsTAATA
NM_000317.3:c.84-79_84-75delinsTAATA MANE Select NP_000308.1:n.84-79_84-75delinsTAATA