Canonical Allele Identifier: CA2000619805

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233174G= , CM000673.2:g.112233174G=	GRCh38
NC_000011.9:g.112103897G= , CM000673.1:g.112103897G=	GRCh37
NC_000011.8:g.111609107G=	NCBI36
NG_008743.1:g.11810G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.255G= MANE Select	ENSP00000280362.3:p.Met85=
ENST00000280362.7:c.255G=	ENSP00000280362.3:p.Met85=
ENST00000524931.1:c.51G=	ENSP00000434688.1:p.Met17=
ENST00000525803.1:c.175G=	ENSP00000431750.1:p.Ala59=
ENST00000527428.5:n.429G=
ENST00000527635.1:n.296G=
ENST00000528679.5:c.*64G=	ENSP00000435895.1:n.*64G=
ENST00000531175.1:n.206G=
ENST00000531673.5:c.*64G=	ENSP00000433469.1:n.*64G=
NM_000317.2:c.255G=	NP_000308.1:p.Met85=
XM_011542943.1:c.216G=	XP_011541245.1:p.Met72=
NM_000317.3:c.255G= MANE Select	NP_000308.1:p.Met85=