Canonical Allele Identifier: CA476797220
Gene: PTS HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.112097232G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112226509G>T , CM000673.2:g.112226509G>T GRCh38
NC_000011.9:g.112097232G>T , CM000673.1:g.112097232G>T GRCh37
NC_000011.8:g.111602442G>T NCBI36
NG_008743.1:g.5145G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.8:c.66G>T MANE Select ENSP00000280362.3:p.Ala22=
ENST00000280362.7:c.66G>T ENSP00000280362.3:p.Ala22=
ENST00000525645.1:n.141G>T
ENST00000525803.1:c.66G>T ENSP00000431750.1:p.Ala22=
ENST00000528679.5:c.66G>T ENSP00000435895.1:p.Ala22=
ENST00000531673.5:c.66G>T ENSP00000433469.1:p.Ala22=
NM_000317.2:c.66G>T NP_000308.1:p.Ala22=
NM_000317.3:c.66G>T MANE Select NP_000308.1:p.Ala22=