Canonical Allele Identifier: CA2206158082

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8847775G= , CM000678.2:g.8847775G=	GRCh38
NC_000016.9:g.8941632G= , CM000678.1:g.8941632G=	GRCh37
NC_000016.8:g.8849133G=	NCBI36
NG_009209.1:g.54963G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.3859G=
ENST00000682393.1:c.*258-1594G=	ENSP00000506774.1:n.*258-1594G=
ENST00000683094.1:c.*262-1594G=	ENSP00000508230.1:n.*262-1594G=
ENST00000683274.1:c.*180-1594G=	ENSP00000507262.1:n.*180-1594G=
ENST00000683435.1:c.*587G=	ENSP00000508092.1:n.*587G=
ENST00000268261.9:c.691G= MANE Select	ENSP00000268261.4:p.Val231=
ENST00000268261.8:c.691G=	ENSP00000268261.4:p.Val231=
ENST00000562025.1:n.225G=
ENST00000562318.5:c.*413G=	ENSP00000454395.1:n.*413G=
ENST00000565221.5:c.*309G=	ENSP00000457932.1:n.*309G=
ENST00000566540.5:c.*313G=	ENSP00000454284.1:n.*313G=
ENST00000566604.5:c.*231G=	ENSP00000456774.1:n.*231G=
ENST00000566983.5:c.610G=	ENSP00000457956.1:p.Val204=
ENST00000567697.1:n.3859G=
ENST00000569958.5:c.418G=	ENSP00000456302.1:p.Val140=
ENST00000570076.5:c.*149G=	ENSP00000456961.1:n.*149G=
NM_000303.2:c.691G=	NP_000294.1:p.Val231=
XM_005255374.3:c.442G=	XP_005255431.1:p.Val148=
XM_011522538.1:c.640-7259G=	XP_011520840.1:n.640-7259G=
XM_005255374.4:c.442G=	XP_005255431.1:p.Val148=
NM_000303.3:c.691G= MANE Select	NP_000294.1:p.Val231=