Canonical Allele Identifier: CA2000619819

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233205G= , CM000673.2:g.112233205G=	GRCh38
NC_000011.9:g.112103928G= , CM000673.1:g.112103928G=	GRCh37
NC_000011.8:g.111609138G=	NCBI36
NG_008743.1:g.11841G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000317.3:c.286G= MANE Select	NP_000308.1:p.Asp96=
ENST00000280362.8:c.286G= MANE Select	ENSP00000280362.3:p.Asp96=
NM_000317.2:c.286G=	NP_000308.1:p.Asp96=
ENST00000280362.7:c.286G=	ENSP00000280362.3:p.Asp96=
ENST00000524931.1:c.82G=	ENSP00000434688.1:p.Asp28=
ENST00000525803.1:c.*20G=	ENSP00000431750.1:n.*20G=
ENST00000527428.5:n.460G=
ENST00000527635.1:n.327G=
ENST00000528679.5:c.*95G=	ENSP00000435895.1:n.*95G=
ENST00000531175.1:n.237G=
ENST00000531673.5:c.*95G=	ENSP00000433469.1:n.*95G=
XM_011542943.1:c.247G=	XP_011541245.1:p.Asp83=