Canonical Allele Identifier: CA277500672

Gene: PMM2

Linked Data

• ClinVar Variation Id: 886920
• ClinVar RCV Id: RCV001119367
• dbSNP Id: rs866278750
• gnomAD v2: 16-8941924-C-T
• gnomAD v3: 16-8848067-C-T
• gnomAD v4: 16-8848067-C-T
• MyVariant Identifiers: chr16:g.8941924C>T (hg19) ; chr16:g.8848067C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8848067C>T , CM000678.2:g.8848067C>T	GRCh38
NC_000016.9:g.8941924C>T , CM000678.1:g.8941924C>T	GRCh37
NC_000016.8:g.8849425C>T	NCBI36
NG_009209.1:g.55255C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.4151C>T
ENST00000682393.1:c.*258-1302C>T	ENSP00000506774.1:n.*258-1302C>T
ENST00000683094.1:c.*262-1302C>T	ENSP00000508230.1:n.*262-1302C>T
ENST00000683274.1:c.*180-1302C>T	ENSP00000507262.1:n.*180-1302C>T
ENST00000268261.9:c.*242C>T MANE Select	ENSP00000268261.4:n.*242C>T
ENST00000268261.8:c.*242C>T	ENSP00000268261.4:n.*242C>T
ENST00000562025.1:n.517C>T
ENST00000566540.5:c.*605C>T	ENSP00000454284.1:n.*605C>T
ENST00000566604.5:c.*523C>T	ENSP00000456774.1:n.*523C>T
ENST00000567697.1:n.4151C>T
ENST00000570076.5:c.*441C>T	ENSP00000456961.1:n.*441C>T
NM_000303.2:c.*242C>T	NP_000294.1:n.*242C>T
XM_005255374.3:c.*242C>T	XP_005255431.1:n.*242C>T
XM_011522538.1:c.640-6967C>T	XP_011520840.1:n.640-6967C>T
XM_005255374.4:c.*242C>T	XP_005255431.1:n.*242C>T
NM_000303.3:c.*242C>T MANE Select	NP_000294.1:n.*242C>T