Canonical Allele Identifier: CA974429289

Gene: PMM2

Linked Data

• dbSNP Id: rs2060939982
• gnomAD v3: 16-8848057-T-TGC
• gnomAD v4: 16-8848057-T-TGC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8848057_8848058insGC , CM000678.2:g.8848057_8848058insGC	GRCh38
NC_000016.9:g.8941914_8941915insGC , CM000678.1:g.8941914_8941915insGC	GRCh37
NC_000016.8:g.8849415_8849416insGC	NCBI36
NG_009209.1:g.55245_55246insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.4141_4142insGC
ENST00000682393.1:c.*258-1312_*258-1311insGC	ENSP00000506774.1:n.*258-1312_*258-1311insGC
ENST00000683094.1:c.*262-1312_*262-1311insGC	ENSP00000508230.1:n.*262-1312_*262-1311insGC
ENST00000683274.1:c.*180-1312_*180-1311insGC	ENSP00000507262.1:n.*180-1312_*180-1311insGC
ENST00000268261.9:c.*232_*233insGC MANE Select	ENSP00000268261.4:n.*232_*233insGC
ENST00000268261.8:c.*232_*233insGC	ENSP00000268261.4:n.*232_*233insGC
ENST00000562025.1:n.507_508insGC
ENST00000566540.5:c.*595_*596insGC	ENSP00000454284.1:n.*595_*596insGC
ENST00000566604.5:c.*513_*514insGC	ENSP00000456774.1:n.*513_*514insGC
ENST00000567697.1:n.4141_4142insGC
ENST00000570076.5:c.*431_*432insGC	ENSP00000456961.1:n.*431_*432insGC
NM_000303.2:c.*232_*233insGC	NP_000294.1:n.*232_*233insGC
XM_005255374.3:c.*232_*233insGC	XP_005255431.1:n.*232_*233insGC
XM_011522538.1:c.640-6977_640-6976insGC	XP_011520840.1:n.640-6977_640-6976insGC
XM_005255374.4:c.*232_*233insGC	XP_005255431.1:n.*232_*233insGC
NM_000303.3:c.*232_*233insGC MANE Select	NP_000294.1:n.*232_*233insGC