Canonical Allele Identifier: CA382627039
Gene: PTS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228629T>A , CM000673.2:g.112228629T>A GRCh38
NC_000011.9:g.112099352T>A , CM000673.1:g.112099352T>A GRCh37
NC_000011.8:g.111604562T>A NCBI36
NG_008743.1:g.7265T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.8:c.119T>A MANE Select ENSP00000280362.3:p.Phe40Tyr
ENST00000280362.7:c.119T>A ENSP00000280362.3:p.Phe40Tyr
ENST00000524931.1:c.-86T>A ENSP00000434688.1:n.-86T>A
ENST00000525645.1:n.194T>A
ENST00000525803.1:c.119T>A ENSP00000431750.1:p.Phe40Tyr
ENST00000528679.5:c.119T>A ENSP00000435895.1:p.Phe40Tyr
ENST00000531673.5:c.119T>A ENSP00000433469.1:p.Phe40Tyr
NM_000317.2:c.119T>A NP_000308.1:p.Phe40Tyr
NM_000317.3:c.119T>A MANE Select NP_000308.1:p.Phe40Tyr