Canonical Allele Identifier: CA2000619941
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112233472C= , CM000673.2:g.112233472C= GRCh38
NC_000011.9:g.112104195C= , CM000673.1:g.112104195C= GRCh37
NC_000011.8:g.111609405C= NCBI36
NG_008743.1:g.12108C=

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.355C= MANE Select ENSP00000280362.3:p.Gln119=
ENST00000280362.7:c.355C= ENSP00000280362.3:p.Gln119=
ENST00000524931.1:c.151C= ENSP00000434688.1:p.Gln51=
ENST00000525803.1:c.*89C= ENSP00000431750.1:n.*89C=
ENST00000527428.5:n.488+239C=
ENST00000527635.1:n.396C=
ENST00000528679.5:c.*164C= ENSP00000435895.1:n.*164C=
ENST00000531673.5:c.*123+239C= ENSP00000433469.1:n.*123+239C=
NM_000317.2:c.355C= NP_000308.1:p.Gln119=
XM_011542943.1:c.316C= XP_011541245.1:p.Gln106=
NM_000317.3:c.355C= MANE Select NP_000308.1:p.Gln119=