Canonical Allele Identifier: CA394689682

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8847803T>G , CM000678.2:g.8847803T>G	GRCh38
NC_000016.9:g.8941660T>G , CM000678.1:g.8941660T>G	GRCh37
NC_000016.8:g.8849161T>G	NCBI36
NG_009209.1:g.54991T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.3887T>G
ENST00000682393.1:c.*258-1566T>G	ENSP00000506774.1:n.*258-1566T>G
ENST00000683094.1:c.*262-1566T>G	ENSP00000508230.1:n.*262-1566T>G
ENST00000683274.1:c.*180-1566T>G	ENSP00000507262.1:n.*180-1566T>G
ENST00000683435.1:c.*615T>G	ENSP00000508092.1:n.*615T>G
ENST00000268261.9:c.719T>G MANE Select	ENSP00000268261.4:p.Ile240Ser
ENST00000268261.8:c.719T>G	ENSP00000268261.4:p.Ile240Ser
ENST00000562025.1:n.253T>G
ENST00000562318.5:c.*441T>G	ENSP00000454395.1:n.*441T>G
ENST00000565221.5:c.*337T>G	ENSP00000457932.1:n.*337T>G
ENST00000566540.5:c.*341T>G	ENSP00000454284.1:n.*341T>G
ENST00000566604.5:c.*259T>G	ENSP00000456774.1:n.*259T>G
ENST00000566983.5:c.638T>G	ENSP00000457956.1:p.Ile213Ser
ENST00000567697.1:n.3887T>G
ENST00000569958.5:c.446T>G	ENSP00000456302.1:p.Ile149Ser
ENST00000570076.5:c.*177T>G	ENSP00000456961.1:n.*177T>G
NM_000303.2:c.719T>G	NP_000294.1:p.Ile240Ser
XM_005255374.3:c.470T>G	XP_005255431.1:p.Ile157Ser
XM_011522538.1:c.640-7231T>G	XP_011520840.1:n.640-7231T>G
XM_005255374.4:c.470T>G	XP_005255431.1:p.Ile157Ser
NM_000303.3:c.719T>G MANE Select	NP_000294.1:p.Ile240Ser