Canonical Allele Identifier: CA2000618598

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112230677A= , CM000673.2:g.112230677A=	GRCh38
NC_000011.9:g.112101400A= , CM000673.1:g.112101400A=	GRCh37
NC_000011.8:g.111606610A=	NCBI36
NG_008743.1:g.9313A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000317.3:c.238A= MANE Select	NP_000308.1:p.Met80=
ENST00000280362.8:c.238A= MANE Select	ENSP00000280362.3:p.Met80=
NM_000317.2:c.238A=	NP_000308.1:p.Met80=
ENST00000280362.7:c.238A=	ENSP00000280362.3:p.Met80=
ENST00000524931.1:c.34A=	ENSP00000434688.1:p.Met12=
ENST00000525803.1:c.163+2004A=	ENSP00000431750.1:n.163+2004A=
ENST00000527428.5:n.412A=
ENST00000527635.1:n.279A=
ENST00000528679.5:c.*47A=	ENSP00000435895.1:n.*47A=
ENST00000531175.1:n.189A=
ENST00000531673.5:c.*47A=	ENSP00000433469.1:n.*47A=
XM_011542943.1:c.199A=	XP_011541245.1:p.Met67=