Canonical Allele Identifier: CA2206158355
Gene: PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8848112G= , CM000678.2:g.8848112G= GRCh38
NC_000016.9:g.8941969G= , CM000678.1:g.8941969G= GRCh37
NC_000016.8:g.8849470G= NCBI36
NG_009209.1:g.55300G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567697.2:n.4196G=
ENST00000682393.1:c.*258-1257G= ENSP00000506774.1:n.*258-1257G=
ENST00000683094.1:c.*262-1257G= ENSP00000508230.1:n.*262-1257G=
ENST00000683274.1:c.*180-1257G= ENSP00000507262.1:n.*180-1257G=
ENST00000268261.9:c.*287G= MANE Select ENSP00000268261.4:n.*287G=
ENST00000268261.8:c.*287G= ENSP00000268261.4:n.*287G=
ENST00000562025.1:n.562G=
ENST00000566540.5:c.*650G= ENSP00000454284.1:n.*650G=
ENST00000566604.5:c.*568G= ENSP00000456774.1:n.*568G=
ENST00000567697.1:n.4196G=
ENST00000570076.5:c.*486G= ENSP00000456961.1:n.*486G=
NM_000303.2:c.*287G= NP_000294.1:n.*287G=
XM_005255374.3:c.*287G= XP_005255431.1:n.*287G=
XM_011522538.1:c.640-6922G= XP_011520840.1:n.640-6922G=
XM_005255374.4:c.*287G= XP_005255431.1:n.*287G=
NM_000303.3:c.*287G= MANE Select NP_000294.1:n.*287G=