Canonical Allele Identifier: CA382627796

Gene: PTS

Linked Data

• MyVariant Identifiers: chr11:g.112103904C>A (hg19) ; chr11:g.112233181C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233181C>A , CM000673.2:g.112233181C>A	GRCh38
NC_000011.9:g.112103904C>A , CM000673.1:g.112103904C>A	GRCh37
NC_000011.8:g.111609114C>A	NCBI36
NG_008743.1:g.11817C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.262C>A MANE Select	ENSP00000280362.3:p.Leu88Ile
ENST00000280362.7:c.262C>A	ENSP00000280362.3:p.Leu88Ile
ENST00000524931.1:c.58C>A	ENSP00000434688.1:p.Leu20Ile
ENST00000525803.1:c.182C>A	ENSP00000431750.1:p.Pro61His
ENST00000527428.5:n.436C>A
ENST00000527635.1:n.303C>A
ENST00000528679.5:c.*71C>A	ENSP00000435895.1:n.*71C>A
ENST00000531175.1:n.213C>A
ENST00000531673.5:c.*71C>A	ENSP00000433469.1:n.*71C>A
NM_000317.2:c.262C>A	NP_000308.1:p.Leu88Ile
XM_011542943.1:c.223C>A	XP_011541245.1:p.Leu75Ile
NM_000317.3:c.262C>A MANE Select	NP_000308.1:p.Leu88Ile