Canonical Allele Identifier: CA2793647395

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112228590_112228591insTTTTT , CM000673.2:g.112228590_112228591insTTTTT	GRCh38
NC_000011.9:g.112099313_112099314insTTTTT , CM000673.1:g.112099313_112099314insTTTTT	GRCh37
NC_000011.8:g.111604523_111604524insTTTTT	NCBI36
NG_008743.1:g.7226_7227insTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.84-4_84-3insTTTTT MANE Select	ENSP00000280362.3:n.84-4_84-3insTTTTT
ENST00000280362.7:c.84-4_84-3insTTTTT	ENSP00000280362.3:n.84-4_84-3insTTTTT
ENST00000524931.1:c.-121-4_-121-3insTTTTT	ENSP00000434688.1:n.-121-4_-121-3insTTTTT
ENST00000525645.1:n.159-4_159-3insTTTTT
ENST00000525803.1:c.84-4_84-3insTTTTT	ENSP00000431750.1:n.84-4_84-3insTTTTT
ENST00000528679.5:c.84-4_84-3insTTTTT	ENSP00000435895.1:n.84-4_84-3insTTTTT
ENST00000531673.5:c.84-4_84-3insTTTTT	ENSP00000433469.1:n.84-4_84-3insTTTTT
NM_000317.2:c.84-4_84-3insTTTTT	NP_000308.1:n.84-4_84-3insTTTTT
NM_000317.3:c.84-4_84-3insTTTTT MANE Select	NP_000308.1:n.84-4_84-3insTTTTT