Canonical Allele Identifier: CA476797622
Gene: PTS HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.112104188C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112233465C>T , CM000673.2:g.112233465C>T GRCh38
NC_000011.9:g.112104188C>T , CM000673.1:g.112104188C>T GRCh37
NC_000011.8:g.111609398C>T NCBI36
NG_008743.1:g.12101C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.348C>T MANE Select ENSP00000280362.3:p.Asp116=
ENST00000280362.7:c.348C>T ENSP00000280362.3:p.Asp116=
ENST00000524931.1:c.144C>T ENSP00000434688.1:p.Asp48=
ENST00000525803.1:c.*82C>T ENSP00000431750.1:n.*82C>T
ENST00000527428.5:n.488+232C>T
ENST00000527635.1:n.389C>T
ENST00000528679.5:c.*157C>T ENSP00000435895.1:n.*157C>T
ENST00000531673.5:c.*123+232C>T ENSP00000433469.1:n.*123+232C>T
NM_000317.2:c.348C>T NP_000308.1:p.Asp116=
XM_011542943.1:c.309C>T XP_011541245.1:p.Asp103=
NM_000317.3:c.348C>T MANE Select NP_000308.1:p.Asp116=