Canonical Allele Identifier: CA2000617645
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228658G= , CM000673.2:g.112228658G= GRCh38
NC_000011.9:g.112099381G= , CM000673.1:g.112099381G= GRCh37
NC_000011.8:g.111604591G= NCBI36
NG_008743.1:g.7294G=

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.148G= MANE Select ENSP00000280362.3:p.Gly50=
ENST00000280362.7:c.148G= ENSP00000280362.3:p.Gly50=
ENST00000524931.1:c.-57G= ENSP00000434688.1:n.-57G=
ENST00000525645.1:n.223G=
ENST00000525803.1:c.148G= ENSP00000431750.1:p.Gly50=
ENST00000528679.5:c.148G= ENSP00000435895.1:p.Gly50=
ENST00000531673.5:c.148G= ENSP00000433469.1:p.Gly50=
NM_000317.2:c.148G= NP_000308.1:p.Gly50=
NM_000317.3:c.148G= MANE Select NP_000308.1:p.Gly50=