Canonical Allele Identifier: CA2616001382

Gene: PTS

Linked Data

• gnomAD v4: 11-112233024-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233025del , CM000673.2:g.112233025del	GRCh38
NC_000011.9:g.112103748del , CM000673.1:g.112103748del	GRCh37
NC_000011.8:g.111608958del	NCBI36
NG_008743.1:g.11661del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.244-138del MANE Select	ENSP00000280362.3:n.244-138del
ENST00000280362.7:c.244-138del	ENSP00000280362.3:n.244-138del
ENST00000524931.1:c.40-138del	ENSP00000434688.1:n.40-138del
ENST00000525803.1:c.164-138del	ENSP00000431750.1:n.164-138del
ENST00000527428.5:n.418-138del
ENST00000527635.1:n.285-138del
ENST00000528679.5:c.*53-138del	ENSP00000435895.1:n.*53-138del
ENST00000531175.1:n.195-138del
ENST00000531673.5:c.*53-138del	ENSP00000433469.1:n.*53-138del
NM_000317.2:c.244-138del	NP_000308.1:n.244-138del
XM_011542943.1:c.205-138del	XP_011541245.1:n.205-138del
NM_000317.3:c.244-138del MANE Select	NP_000308.1:n.244-138del