Canonical Allele Identifier: CA16041796
Gene: PMM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 370776
ClinVar RCV Id: RCV000408959
dbSNP Id: rs1057516757

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8806405dup , CM000678.2:g.8806405dup GRCh38
NC_000016.9:g.8900262dup , CM000678.1:g.8900262dup GRCh37
NC_000016.8:g.8807763dup NCBI36
NG_009209.1:g.13593dup

Transcript Alleles

HGVS Amino-acid change
ENST00000682008.1:c.345dup ENSP00000507849.1:p.Arg116GlufsTer6
ENST00000682393.1:c.178+4495dup ENSP00000506774.1:n.178+4495dup
ENST00000683094.1:c.*67dup ENSP00000508230.1:n.*67dup
ENST00000683274.1:c.345dup ENSP00000507262.1:p.Arg116GlufsTer?
ENST00000683435.1:c.*341dup ENSP00000508092.1:n.*341dup
ENST00000268261.9:c.345dup MANE Select ENSP00000268261.4:p.Arg116GlufsTer6
ENST00000268261.8:c.345dup ENSP00000268261.4:p.Arg116GlufsTer6
ENST00000562318.5:c.*67dup ENSP00000454395.1:n.*67dup
ENST00000562448.1:n.309dup
ENST00000564030.5:n.407dup
ENST00000564069.1:c.316dup
ENST00000565221.5:c.178+4495dup ENSP00000457932.1:n.178+4495dup
ENST00000565896.5:c.*145+4016dup ENSP00000456024.1:n.*145+4016dup
ENST00000566540.5:c.*67dup ENSP00000454284.1:n.*67dup
ENST00000566604.5:c.345dup ENSP00000456774.1:p.Arg116GlufsTer?
ENST00000566983.5:c.264dup ENSP00000457956.1:p.Arg89GlufsTer6
ENST00000568602.5:c.*198dup ENSP00000455066.1:n.*198dup
ENST00000569958.5:c.178+4495dup ENSP00000456302.1:n.178+4495dup
ENST00000570076.5:c.178+4495dup ENSP00000456961.1:n.178+4495dup
ENST00000570134.5:c.*67dup ENSP00000456275.1:n.*67dup
NM_000303.2:c.345dup NP_000294.1:p.Arg116GlufsTer6
XM_005255372.3:c.345dup XP_005255429.1:p.Arg116GlufsTer6
XM_005255373.3:c.96dup XP_005255430.1:p.Arg33GlufsTer6
XM_005255374.3:c.96dup XP_005255431.1:p.Arg33GlufsTer6
XM_011522538.1:c.345dup XP_011520840.1:p.Arg116GlufsTer6
XM_011522539.1:c.-29+4495dup XP_011520841.1:n.-29+4495dup
XM_005255374.4:c.96dup XP_005255431.1:p.Arg33GlufsTer6
NM_000303.3:c.345dup MANE Select NP_000294.1:p.Arg116GlufsTer6