Canonical Allele Identifier: CA2000617613
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228590_112228597delinsTCAGTAAA , CM000673.2:g.112228590_112228597delinsTCAGTAAA GRCh38
NC_000011.9:g.112099313_112099320delinsTCAGTAAA , CM000673.1:g.112099313_112099320delinsTCAGTAAA GRCh37
NC_000011.8:g.111604523_111604530delinsTCAGTAAA NCBI36
NG_008743.1:g.7226_7233delinsTCAGTAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.8:c.84-4_87delinsTCAGTAAA
ENST00000280362.7:c.84-4_87delinsTCAGTAAA
ENST00000524931.1:c.-121-4_-118delinsTCAGTAAA
ENST00000525645.1:n.159-4_162delinsTCAGTAAA
ENST00000525803.1:c.84-4_87delinsTCAGTAAA
ENST00000528679.5:c.84-4_87delinsTCAGTAAA
ENST00000531673.5:c.84-4_87delinsTCAGTAAA
NM_000317.2:c.84-4_87delinsTCAGTAAA
NM_000317.3:c.84-4_87delinsTCAGTAAA