Canonical Allele Identifier: CA2602769780

Gene: PTS

Linked Data

• gnomAD v3: 11-112233139-A-AT
• gnomAD v4: 11-112233139-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233143dup , CM000673.2:g.112233143dup	GRCh38
NC_000011.9:g.112103866dup , CM000673.1:g.112103866dup	GRCh37
NC_000011.8:g.111609076dup	NCBI36
NG_008743.1:g.11779dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.244-20dup MANE Select	ENSP00000280362.3:n.244-20dup
ENST00000280362.7:c.244-20dup	ENSP00000280362.3:n.244-20dup
ENST00000524931.1:c.40-20dup	ENSP00000434688.1:n.40-20dup
ENST00000525803.1:c.164-20dup	ENSP00000431750.1:n.164-20dup
ENST00000527428.5:n.418-20dup
ENST00000527635.1:n.285-20dup
ENST00000528679.5:c.*53-20dup	ENSP00000435895.1:n.*53-20dup
ENST00000531175.1:n.195-20dup
ENST00000531673.5:c.*53-20dup	ENSP00000433469.1:n.*53-20dup
NM_000317.2:c.244-20dup	NP_000308.1:n.244-20dup
XM_011542943.1:c.205-20dup	XP_011541245.1:n.205-20dup
NM_000317.3:c.244-20dup MANE Select	NP_000308.1:n.244-20dup