Canonical Allele Identifier: CA2000619727
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112233016A= , CM000673.2:g.112233016A= GRCh38
NC_000011.9:g.112103739A= , CM000673.1:g.112103739A= GRCh37
NC_000011.8:g.111608949A= NCBI36
NG_008743.1:g.11652A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.8:c.244-147A= MANE Select ENSP00000280362.3:n.244-147A=
ENST00000280362.7:c.244-147A= ENSP00000280362.3:n.244-147A=
ENST00000524931.1:c.40-147A= ENSP00000434688.1:n.40-147A=
ENST00000525803.1:c.164-147A= ENSP00000431750.1:n.164-147A=
ENST00000527428.5:n.418-147A=
ENST00000527635.1:n.285-147A=
ENST00000528679.5:c.*53-147A= ENSP00000435895.1:n.*53-147A=
ENST00000531175.1:n.195-147A=
ENST00000531673.5:c.*53-147A= ENSP00000433469.1:n.*53-147A=
NM_000317.2:c.244-147A= NP_000308.1:n.244-147A=
XM_011542943.1:c.205-147A= XP_011541245.1:n.205-147A=
NM_000317.3:c.244-147A= MANE Select NP_000308.1:n.244-147A=