Canonical Allele Identifier: CA493489709

Gene: PMM2

Linked Data

• gnomAD v4: 16-8847942-T-C
• MyVariant Identifiers: chr16:g.8941799T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8847942T>C , CM000678.2:g.8847942T>C	GRCh38
NC_000016.9:g.8941799T>C , CM000678.1:g.8941799T>C	GRCh37
NC_000016.8:g.8849300T>C	NCBI36
NG_009209.1:g.55130T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.4026T>C
ENST00000682393.1:c.*258-1427T>C	ENSP00000506774.1:n.*258-1427T>C
ENST00000683094.1:c.*262-1427T>C	ENSP00000508230.1:n.*262-1427T>C
ENST00000683274.1:c.*180-1427T>C	ENSP00000507262.1:n.*180-1427T>C
ENST00000683435.1:c.*754T>C	ENSP00000508092.1:n.*754T>C
ENST00000268261.9:c.*117T>C MANE Select	ENSP00000268261.4:n.*117T>C
ENST00000268261.8:c.*117T>C	ENSP00000268261.4:n.*117T>C
ENST00000562025.1:n.392T>C
ENST00000562318.5:c.*580T>C	ENSP00000454395.1:n.*580T>C
ENST00000565221.5:c.*476T>C	ENSP00000457932.1:n.*476T>C
ENST00000566540.5:c.*480T>C	ENSP00000454284.1:n.*480T>C
ENST00000566604.5:c.*398T>C	ENSP00000456774.1:n.*398T>C
ENST00000567697.1:n.4026T>C
ENST00000569958.5:c.*117T>C	ENSP00000456302.1:n.*117T>C
ENST00000570076.5:c.*316T>C	ENSP00000456961.1:n.*316T>C
NM_000303.2:c.*117T>C	NP_000294.1:n.*117T>C
XM_005255374.3:c.*117T>C	XP_005255431.1:n.*117T>C
XM_011522538.1:c.640-7092T>C	XP_011520840.1:n.640-7092T>C
XM_005255374.4:c.*117T>C	XP_005255431.1:n.*117T>C
NM_000303.3:c.*117T>C MANE Select	NP_000294.1:n.*117T>C