Canonical Allele Identifier: CA6278442
Gene: PTS HGNC NCBI

Linked Data

dbSNP Id: rs755535312

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228564A>T , CM000673.2:g.112228564A>T GRCh38
NC_000011.9:g.112099287A>T , CM000673.1:g.112099287A>T GRCh37
NC_000011.8:g.111604497A>T NCBI36
NG_008743.1:g.7200A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.84-30A>T MANE Select ENSP00000280362.3:n.84-30A>T
ENST00000280362.7:c.84-30A>T ENSP00000280362.3:n.84-30A>T
ENST00000524931.1:c.-121-30A>T ENSP00000434688.1:n.-121-30A>T
ENST00000525645.1:n.159-30A>T
ENST00000525803.1:c.84-30A>T ENSP00000431750.1:n.84-30A>T
ENST00000528679.5:c.84-30A>T ENSP00000435895.1:n.84-30A>T
ENST00000531673.5:c.84-30A>T ENSP00000433469.1:n.84-30A>T
NM_000317.2:c.84-30A>T NP_000308.1:n.84-30A>T
NM_000317.3:c.84-30A>T MANE Select NP_000308.1:n.84-30A>T