Canonical Allele Identifier: CA2000617556
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228461C= , CM000673.2:g.112228461C= GRCh38
NC_000011.9:g.112099184C= , CM000673.1:g.112099184C= GRCh37
NC_000011.8:g.111604394C= NCBI36
NG_008743.1:g.7097C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.8:c.84-133C= MANE Select ENSP00000280362.3:n.84-133C=
ENST00000280362.7:c.84-133C= ENSP00000280362.3:n.84-133C=
ENST00000524931.1:c.-122+103C= ENSP00000434688.1:n.-122+103C=
ENST00000525645.1:n.159-133C=
ENST00000525803.1:c.84-133C= ENSP00000431750.1:n.84-133C=
ENST00000528679.5:c.84-133C= ENSP00000435895.1:n.84-133C=
ENST00000531673.5:c.84-133C= ENSP00000433469.1:n.84-133C=
NM_000317.2:c.84-133C= NP_000308.1:n.84-133C=
NM_000317.3:c.84-133C= MANE Select NP_000308.1:n.84-133C=