Canonical Allele Identifier: CA382627889

Gene: PTS

Linked Data

• MyVariant Identifiers: chr11:g.112103941T>A (hg19) ; chr11:g.112233218T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233218T>A , CM000673.2:g.112233218T>A	GRCh38
NC_000011.9:g.112103941T>A , CM000673.1:g.112103941T>A	GRCh37
NC_000011.8:g.111609151T>A	NCBI36
NG_008743.1:g.11854T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.299T>A MANE Select	ENSP00000280362.3:p.Phe100Tyr
ENST00000280362.7:c.299T>A	ENSP00000280362.3:p.Phe100Tyr
ENST00000524931.1:c.95T>A	ENSP00000434688.1:p.Phe32Tyr
ENST00000525803.1:c.*33T>A	ENSP00000431750.1:n.*33T>A
ENST00000527428.5:n.473T>A
ENST00000527635.1:n.340T>A
ENST00000528679.5:c.*108T>A	ENSP00000435895.1:n.*108T>A
ENST00000531175.1:n.250T>A
ENST00000531673.5:c.*108T>A	ENSP00000433469.1:n.*108T>A
NM_000317.2:c.299T>A	NP_000308.1:p.Phe100Tyr
XM_011542943.1:c.260T>A	XP_011541245.1:p.Phe87Tyr
NM_000317.3:c.299T>A MANE Select	NP_000308.1:p.Phe100Tyr