Canonical Allele Identifier: CA2000616478
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112226402G= , CM000673.2:g.112226402G= GRCh38
NC_000011.9:g.112097125G= , CM000673.1:g.112097125G= GRCh37
NC_000011.8:g.111602335G= NCBI36
NG_008743.1:g.5038G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.7:c.-42G= ENSP00000280362.3:n.-42G=
ENST00000525645.1:n.34G=
ENST00000528679.5:c.-42G= ENSP00000435895.1:n.-42G=
ENST00000531673.5:c.-42G= ENSP00000433469.1:n.-42G=
NM_000317.2:c.-42G= NP_000308.1:n.-42G=