Canonical Allele Identifier: CA2000619938
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112233464A= , CM000673.2:g.112233464A= GRCh38
NC_000011.9:g.112104187A= , CM000673.1:g.112104187A= GRCh37
NC_000011.8:g.111609397A= NCBI36
NG_008743.1:g.12100A=

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.347A= MANE Select ENSP00000280362.3:p.Asp116=
ENST00000280362.7:c.347A= ENSP00000280362.3:p.Asp116=
ENST00000524931.1:c.143A= ENSP00000434688.1:p.Asp48=
ENST00000525803.1:c.*81A= ENSP00000431750.1:n.*81A=
ENST00000527428.5:n.488+231A=
ENST00000527635.1:n.388A=
ENST00000528679.5:c.*156A= ENSP00000435895.1:n.*156A=
ENST00000531673.5:c.*123+231A= ENSP00000433469.1:n.*123+231A=
NM_000317.2:c.347A= NP_000308.1:p.Asp116=
XM_011542943.1:c.308A= XP_011541245.1:p.Asp103=
NM_000317.3:c.347A= MANE Select NP_000308.1:p.Asp116=