Canonical Allele Identifier: CA2793651163
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112233231_112233234del , CM000673.2:g.112233231_112233234del GRCh38
NC_000011.9:g.112103954_112103957del , CM000673.1:g.112103954_112103957del GRCh37
NC_000011.8:g.111609164_111609167del NCBI36
NG_008743.1:g.11867_11870del

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.8:c.312_314+1del
ENST00000280362.7:c.312_314+1del
ENST00000524931.1:c.108_110+1del
ENST00000525803.1:c.*46_*48+1del
ENST00000527428.5:n.486_488+1del
ENST00000527635.1:n.353_355+1del
ENST00000528679.5:c.*121_*123+1del
ENST00000531175.1:n.263_266del
ENST00000531673.5:c.*121_*123+1del
NM_000317.2:c.312_314+1del
XM_011542943.1:c.273_275+1del
NM_000317.3:c.312_314+1del