Canonical Allele Identifier: CA493489696

Gene: PMM2

Linked Data

• MyVariant Identifiers: chr16:g.8941794C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8847937C>T , CM000678.2:g.8847937C>T	GRCh38
NC_000016.9:g.8941794C>T , CM000678.1:g.8941794C>T	GRCh37
NC_000016.8:g.8849295C>T	NCBI36
NG_009209.1:g.55125C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.4021C>T
ENST00000682393.1:c.*258-1432C>T	ENSP00000506774.1:n.*258-1432C>T
ENST00000683094.1:c.*262-1432C>T	ENSP00000508230.1:n.*262-1432C>T
ENST00000683274.1:c.*180-1432C>T	ENSP00000507262.1:n.*180-1432C>T
ENST00000683435.1:c.*749C>T	ENSP00000508092.1:n.*749C>T
ENST00000268261.9:c.*112C>T MANE Select	ENSP00000268261.4:n.*112C>T
ENST00000268261.8:c.*112C>T	ENSP00000268261.4:n.*112C>T
ENST00000562025.1:n.387C>T
ENST00000562318.5:c.*575C>T	ENSP00000454395.1:n.*575C>T
ENST00000565221.5:c.*471C>T	ENSP00000457932.1:n.*471C>T
ENST00000566540.5:c.*475C>T	ENSP00000454284.1:n.*475C>T
ENST00000566604.5:c.*393C>T	ENSP00000456774.1:n.*393C>T
ENST00000567697.1:n.4021C>T
ENST00000569958.5:c.*112C>T	ENSP00000456302.1:n.*112C>T
ENST00000570076.5:c.*311C>T	ENSP00000456961.1:n.*311C>T
NM_000303.2:c.*112C>T	NP_000294.1:n.*112C>T
XM_005255374.3:c.*112C>T	XP_005255431.1:n.*112C>T
XM_011522538.1:c.640-7097C>T	XP_011520840.1:n.640-7097C>T
XM_005255374.4:c.*112C>T	XP_005255431.1:n.*112C>T
NM_000303.3:c.*112C>T MANE Select	NP_000294.1:n.*112C>T