Canonical Allele Identifier: CA2805787674

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8848029C>A , CM000678.2:g.8848029C>A	GRCh38
NC_000016.9:g.8941886C>A , CM000678.1:g.8941886C>A	GRCh37
NC_000016.8:g.8849387C>A	NCBI36
NG_009209.1:g.55217C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.4113C>A
ENST00000682393.1:c.*258-1340C>A	ENSP00000506774.1:n.*258-1340C>A
ENST00000683094.1:c.*262-1340C>A	ENSP00000508230.1:n.*262-1340C>A
ENST00000683274.1:c.*180-1340C>A	ENSP00000507262.1:n.*180-1340C>A
ENST00000268261.9:c.*204C>A MANE Select	ENSP00000268261.4:n.*204C>A
ENST00000268261.8:c.*204C>A	ENSP00000268261.4:n.*204C>A
ENST00000562025.1:n.479C>A
ENST00000562318.5:c.*667C>A	ENSP00000454395.1:n.*667C>A
ENST00000565221.5:c.*563C>A	ENSP00000457932.1:n.*563C>A
ENST00000566540.5:c.*567C>A	ENSP00000454284.1:n.*567C>A
ENST00000566604.5:c.*485C>A	ENSP00000456774.1:n.*485C>A
ENST00000567697.1:n.4113C>A
ENST00000569958.5:c.*204C>A	ENSP00000456302.1:n.*204C>A
ENST00000570076.5:c.*403C>A	ENSP00000456961.1:n.*403C>A
NM_000303.2:c.*204C>A	NP_000294.1:n.*204C>A
XM_005255374.3:c.*204C>A	XP_005255431.1:n.*204C>A
XM_011522538.1:c.640-7005C>A	XP_011520840.1:n.640-7005C>A
XM_005255374.4:c.*204C>A	XP_005255431.1:n.*204C>A
NM_000303.3:c.*204C>A MANE Select	NP_000294.1:n.*204C>A