Canonical Allele Identifier: CA974429270

Gene: PMM2

Linked Data

• gnomAD v3: 16-8848057-T-TGG
• gnomAD v4: 16-8848057-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8848057_8848058insGG , CM000678.2:g.8848057_8848058insGG	GRCh38
NC_000016.9:g.8941914_8941915insGG , CM000678.1:g.8941914_8941915insGG	GRCh37
NC_000016.8:g.8849415_8849416insGG	NCBI36
NG_009209.1:g.55245_55246insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.4141_4142insGG
ENST00000682393.1:c.*258-1312_*258-1311insGG	ENSP00000506774.1:n.*258-1312_*258-1311insGG
ENST00000683094.1:c.*262-1312_*262-1311insGG	ENSP00000508230.1:n.*262-1312_*262-1311insGG
ENST00000683274.1:c.*180-1312_*180-1311insGG	ENSP00000507262.1:n.*180-1312_*180-1311insGG
ENST00000268261.9:c.*232_*233insGG MANE Select	ENSP00000268261.4:n.*232_*233insGG
ENST00000268261.8:c.*232_*233insGG	ENSP00000268261.4:n.*232_*233insGG
ENST00000562025.1:n.507_508insGG
ENST00000566540.5:c.*595_*596insGG	ENSP00000454284.1:n.*595_*596insGG
ENST00000566604.5:c.*513_*514insGG	ENSP00000456774.1:n.*513_*514insGG
ENST00000567697.1:n.4141_4142insGG
ENST00000570076.5:c.*431_*432insGG	ENSP00000456961.1:n.*431_*432insGG
NM_000303.2:c.*232_*233insGG	NP_000294.1:n.*232_*233insGG
XM_005255374.3:c.*232_*233insGG	XP_005255431.1:n.*232_*233insGG
XM_011522538.1:c.640-6977_640-6976insGG	XP_011520840.1:n.640-6977_640-6976insGG
XM_005255374.4:c.*232_*233insGG	XP_005255431.1:n.*232_*233insGG
NM_000303.3:c.*232_*233insGG MANE Select	NP_000294.1:n.*232_*233insGG