Canonical Allele Identifier: CA493489866

Gene: PMM2

Linked Data

• dbSNP Id: rs1274332103
• gnomAD v3: 16-8848111-T-C
• gnomAD v4: 16-8848111-T-C
• MyVariant Identifiers: chr16:g.8941968T>C (hg19) ; chr16:g.8848111T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8848111T>C , CM000678.2:g.8848111T>C	GRCh38
NC_000016.9:g.8941968T>C , CM000678.1:g.8941968T>C	GRCh37
NC_000016.8:g.8849469T>C	NCBI36
NG_009209.1:g.55299T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.4195T>C
ENST00000682393.1:c.*258-1258T>C	ENSP00000506774.1:n.*258-1258T>C
ENST00000683094.1:c.*262-1258T>C	ENSP00000508230.1:n.*262-1258T>C
ENST00000683274.1:c.*180-1258T>C	ENSP00000507262.1:n.*180-1258T>C
ENST00000268261.9:c.*286T>C MANE Select	ENSP00000268261.4:n.*286T>C
ENST00000268261.8:c.*286T>C	ENSP00000268261.4:n.*286T>C
ENST00000562025.1:n.561T>C
ENST00000566540.5:c.*649T>C	ENSP00000454284.1:n.*649T>C
ENST00000566604.5:c.*567T>C	ENSP00000456774.1:n.*567T>C
ENST00000567697.1:n.4195T>C
ENST00000570076.5:c.*485T>C	ENSP00000456961.1:n.*485T>C
NM_000303.2:c.*286T>C	NP_000294.1:n.*286T>C
XM_005255374.3:c.*286T>C	XP_005255431.1:n.*286T>C
XM_011522538.1:c.640-6923T>C	XP_011520840.1:n.640-6923T>C
XM_005255374.4:c.*286T>C	XP_005255431.1:n.*286T>C
NM_000303.3:c.*286T>C MANE Select	NP_000294.1:n.*286T>C