Canonical Allele Identifier: CA2206158321

Gene: PMM2

Linked Data

• dbSNP Id: rs2060940357
• gnomAD v4: 16-8848091-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8848091C>A , CM000678.2:g.8848091C>A	GRCh38
NC_000016.9:g.8941948C>A , CM000678.1:g.8941948C>A	GRCh37
NC_000016.8:g.8849449C>A	NCBI36
NG_009209.1:g.55279C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.4175C>A
ENST00000682393.1:c.*258-1278C>A	ENSP00000506774.1:n.*258-1278C>A
ENST00000683094.1:c.*262-1278C>A	ENSP00000508230.1:n.*262-1278C>A
ENST00000683274.1:c.*180-1278C>A	ENSP00000507262.1:n.*180-1278C>A
ENST00000268261.9:c.*266C>A MANE Select	ENSP00000268261.4:n.*266C>A
ENST00000268261.8:c.*266C>A	ENSP00000268261.4:n.*266C>A
ENST00000562025.1:n.541C>A
ENST00000566540.5:c.*629C>A	ENSP00000454284.1:n.*629C>A
ENST00000566604.5:c.*547C>A	ENSP00000456774.1:n.*547C>A
ENST00000567697.1:n.4175C>A
ENST00000570076.5:c.*465C>A	ENSP00000456961.1:n.*465C>A
NM_000303.2:c.*266C>A	NP_000294.1:n.*266C>A
XM_005255374.3:c.*266C>A	XP_005255431.1:n.*266C>A
XM_011522538.1:c.640-6943C>A	XP_011520840.1:n.640-6943C>A
XM_005255374.4:c.*266C>A	XP_005255431.1:n.*266C>A
NM_000303.3:c.*266C>A MANE Select	NP_000294.1:n.*266C>A