Canonical Allele Identifier: CA2000616482
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112226406G= , CM000673.2:g.112226406G= GRCh38
NC_000011.9:g.112097129G= , CM000673.1:g.112097129G= GRCh37
NC_000011.8:g.111602339G= NCBI36
NG_008743.1:g.5042G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.7:c.-38G= ENSP00000280362.3:n.-38G=
ENST00000525645.1:n.38G=
ENST00000528679.5:c.-38G= ENSP00000435895.1:n.-38G=
ENST00000531673.5:c.-38G= ENSP00000433469.1:n.-38G=
NM_000317.2:c.-38G= NP_000308.1:n.-38G=