Canonical Allele Identifier: CA2000617583
Gene: PTS HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228546_112228547delinsGA , CM000673.2:g.112228546_112228547delinsGA GRCh38
NC_000011.9:g.112099269_112099270delinsGA , CM000673.1:g.112099269_112099270delinsGA GRCh37
NC_000011.8:g.111604479_111604480delinsGA NCBI36
NG_008743.1:g.7182_7183delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.84-48_84-47delinsGA MANE Select ENSP00000280362.3:n.84-48_84-47delinsGA
ENST00000280362.7:c.84-48_84-47delinsGA ENSP00000280362.3:n.84-48_84-47delinsGA
ENST00000524931.1:c.-121-48_-121-47delinsGA ENSP00000434688.1:n.-121-48_-121-47delins...
ENST00000525645.1:n.159-48_159-47delinsGA
ENST00000525803.1:c.84-48_84-47delinsGA ENSP00000431750.1:n.84-48_84-47delinsGA
ENST00000528679.5:c.84-48_84-47delinsGA ENSP00000435895.1:n.84-48_84-47delinsGA
ENST00000531673.5:c.84-48_84-47delinsGA ENSP00000433469.1:n.84-48_84-47delinsGA
NM_000317.2:c.84-48_84-47delinsGA NP_000308.1:n.84-48_84-47delinsGA
NM_000317.3:c.84-48_84-47delinsGA MANE Select NP_000308.1:n.84-48_84-47delinsGA
Search 100 bp 5'
Search 100 bp 3'