Canonical Allele Identifier: CA2206158211

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8847966G= , CM000678.2:g.8847966G=	GRCh38
NC_000016.9:g.8941823G= , CM000678.1:g.8941823G=	GRCh37
NC_000016.8:g.8849324G=	NCBI36
NG_009209.1:g.55154G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.4050G=
ENST00000682393.1:c.*258-1403G=	ENSP00000506774.1:n.*258-1403G=
ENST00000683094.1:c.*262-1403G=	ENSP00000508230.1:n.*262-1403G=
ENST00000683274.1:c.*180-1403G=	ENSP00000507262.1:n.*180-1403G=
ENST00000268261.9:c.*141G= MANE Select	ENSP00000268261.4:n.*141G=
ENST00000268261.8:c.*141G=	ENSP00000268261.4:n.*141G=
ENST00000562025.1:n.416G=
ENST00000562318.5:c.*604G=	ENSP00000454395.1:n.*604G=
ENST00000565221.5:c.*500G=	ENSP00000457932.1:n.*500G=
ENST00000566540.5:c.*504G=	ENSP00000454284.1:n.*504G=
ENST00000566604.5:c.*422G=	ENSP00000456774.1:n.*422G=
ENST00000567697.1:n.4050G=
ENST00000569958.5:c.*141G=	ENSP00000456302.1:n.*141G=
ENST00000570076.5:c.*340G=	ENSP00000456961.1:n.*340G=
NM_000303.2:c.*141G=	NP_000294.1:n.*141G=
XM_005255374.3:c.*141G=	XP_005255431.1:n.*141G=
XM_011522538.1:c.640-7068G=	XP_011520840.1:n.640-7068G=
XM_005255374.4:c.*141G=	XP_005255431.1:n.*141G=
NM_000303.3:c.*141G= MANE Select	NP_000294.1:n.*141G=