Canonical Allele Identifier: CA2000619839

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233244C= , CM000673.2:g.112233244C=	GRCh38
NC_000011.9:g.112103967C= , CM000673.1:g.112103967C=	GRCh37
NC_000011.8:g.111609177C=	NCBI36
NG_008743.1:g.11880C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.314+11C= MANE Select	ENSP00000280362.3:n.314+11C=
ENST00000280362.7:c.314+11C=	ENSP00000280362.3:n.314+11C=
ENST00000524931.1:c.110+11C=	ENSP00000434688.1:n.110+11C=
ENST00000525803.1:c.*48+11C=	ENSP00000431750.1:n.*48+11C=
ENST00000527428.5:n.488+11C=
ENST00000527635.1:n.355+11C=
ENST00000528679.5:c.*123+11C=	ENSP00000435895.1:n.*123+11C=
ENST00000531175.1:n.276C=
ENST00000531673.5:c.*123+11C=	ENSP00000433469.1:n.*123+11C=
NM_000317.2:c.314+11C=	NP_000308.1:n.314+11C=
XM_011542943.1:c.275+11C=	XP_011541245.1:n.275+11C=
NM_000317.3:c.314+11C= MANE Select	NP_000308.1:n.314+11C=