Canonical Allele Identifier: CA2000619849

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233260G= , CM000673.2:g.112233260G=	GRCh38
NC_000011.9:g.112103983G= , CM000673.1:g.112103983G=	GRCh37
NC_000011.8:g.111609193G=	NCBI36
NG_008743.1:g.11896G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.314+27G= MANE Select	ENSP00000280362.3:n.314+27G=
ENST00000280362.7:c.314+27G=	ENSP00000280362.3:n.314+27G=
ENST00000524931.1:c.110+27G=	ENSP00000434688.1:n.110+27G=
ENST00000525803.1:c.*48+27G=	ENSP00000431750.1:n.*48+27G=
ENST00000527428.5:n.488+27G=
ENST00000527635.1:n.355+27G=
ENST00000528679.5:c.*123+27G=	ENSP00000435895.1:n.*123+27G=
ENST00000531175.1:n.292G=
ENST00000531673.5:c.*123+27G=	ENSP00000433469.1:n.*123+27G=
NM_000317.2:c.314+27G=	NP_000308.1:n.314+27G=
XM_011542943.1:c.275+27G=	XP_011541245.1:n.275+27G=
NM_000317.3:c.314+27G= MANE Select	NP_000308.1:n.314+27G=