Canonical Allele Identifier: CA2000616479
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112226403G= , CM000673.2:g.112226403G= GRCh38
NC_000011.9:g.112097126G= , CM000673.1:g.112097126G= GRCh37
NC_000011.8:g.111602336G= NCBI36
NG_008743.1:g.5039G=

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.7:c.-41G= ENSP00000280362.3:n.-41G=
ENST00000525645.1:n.35G=
ENST00000528679.5:c.-41G= ENSP00000435895.1:n.-41G=
ENST00000531673.5:c.-41G= ENSP00000433469.1:n.-41G=
NM_000317.2:c.-41G= NP_000308.1:n.-41G=