Canonical Allele Identifier: CA493506784

Gene: PMM2

Linked Data

• ClinVar Variation Id: 2852212
• ClinVar RCV Id: RCV003621322
• gnomAD v4: 16-8797945-G-A
• MyVariant Identifiers: chr16:g.8891802G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8797945G>A , CM000678.2:g.8797945G>A	GRCh38
NC_000016.9:g.8891802G>A , CM000678.1:g.8891802G>A	GRCh37
NC_000016.8:g.8799303G>A	NCBI36
NG_009209.1:g.5133G>A
NG_033146.1:g.4704C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682008.1:c.63G>A	ENSP00000507849.1:p.Arg21=
ENST00000682393.1:c.63G>A	ENSP00000506774.1:p.Arg21=
ENST00000683094.1:c.63G>A	ENSP00000508230.1:p.Arg21=
ENST00000683274.1:c.63G>A	ENSP00000507262.1:p.Arg21=
ENST00000683435.1:c.63G>A	ENSP00000508092.1:p.Arg21=
ENST00000268261.9:c.63G>A MANE Select	ENSP00000268261.4:p.Arg21=
ENST00000268261.8:c.63G>A	ENSP00000268261.4:p.Arg21=
ENST00000562318.5:c.63G>A	ENSP00000454395.1:p.Arg21=
ENST00000562448.1:n.104G>A
ENST00000564030.5:n.125G>A
ENST00000564069.1:c.34G>A
ENST00000565221.5:c.63G>A	ENSP00000457932.1:p.Arg21=
ENST00000565896.5:c.63G>A	ENSP00000456024.1:p.Arg21=
ENST00000566196.5:n.107G>A
ENST00000566540.5:c.63G>A	ENSP00000454284.1:p.Arg21=
ENST00000566604.5:c.63G>A	ENSP00000456774.1:p.Arg21=
ENST00000566983.5:c.-15-3854G>A	ENSP00000457956.1:n.-15-3854G>A
ENST00000568602.5:c.63G>A	ENSP00000455066.1:p.Arg21=
ENST00000569958.5:c.63G>A	ENSP00000456302.1:p.Arg21=
ENST00000570076.5:c.63G>A	ENSP00000456961.1:p.Arg21=
ENST00000570134.5:c.63G>A	ENSP00000456275.1:p.Arg21=
NM_000303.2:c.63G>A	NP_000294.1:p.Arg21=
XM_005255372.3:c.63G>A	XP_005255429.1:p.Arg21=
XM_005255373.3:c.-110G>A	XP_005255430.1:n.-110G>A
XM_005255374.3:c.-110G>A	XP_005255431.1:n.-110G>A
XM_011522538.1:c.63G>A	XP_011520840.1:p.Arg21=
XM_005255374.4:c.-110G>A	XP_005255431.1:n.-110G>A
NM_000303.3:c.63G>A MANE Select	NP_000294.1:p.Arg21=