Canonical Allele Identifier: CA2000619818

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233200A= , CM000673.2:g.112233200A=	GRCh38
NC_000011.9:g.112103923A= , CM000673.1:g.112103923A=	GRCh37
NC_000011.8:g.111609133A=	NCBI36
NG_008743.1:g.11836A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.281A= MANE Select	ENSP00000280362.3:p.Asp94=
ENST00000280362.7:c.281A=	ENSP00000280362.3:p.Asp94=
ENST00000524931.1:c.77A=	ENSP00000434688.1:p.Asp26=
ENST00000525803.1:c.*15A=	ENSP00000431750.1:n.*15A=
ENST00000527428.5:n.455A=
ENST00000527635.1:n.322A=
ENST00000528679.5:c.*90A=	ENSP00000435895.1:n.*90A=
ENST00000531175.1:n.232A=
ENST00000531673.5:c.*90A=	ENSP00000433469.1:n.*90A=
NM_000317.2:c.281A=	NP_000308.1:p.Asp94=
XM_011542943.1:c.242A=	XP_011541245.1:p.Asp81=
NM_000317.3:c.281A= MANE Select	NP_000308.1:p.Asp94=