Canonical Allele Identifier: CA2206157954
Gene: PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8847569G= , CM000678.2:g.8847569G= GRCh38
NC_000016.9:g.8941426G= , CM000678.1:g.8941426G= GRCh37
NC_000016.8:g.8848927G= NCBI36
NG_009209.1:g.54757G=

Transcript Alleles

HGVS Amino-acid change
ENST00000567697.2:n.3808-155G=
ENST00000682393.1:c.*258-1800G= ENSP00000506774.1:n.*258-1800G=
ENST00000683094.1:c.*262-1800G= ENSP00000508230.1:n.*262-1800G=
ENST00000683274.1:c.*180-1800G= ENSP00000507262.1:n.*180-1800G=
ENST00000683435.1:c.*536-155G= ENSP00000508092.1:n.*536-155G=
ENST00000268261.9:c.640-155G= MANE Select ENSP00000268261.4:n.640-155G=
ENST00000268261.8:c.640-155G= ENSP00000268261.4:n.640-155G=
ENST00000562025.1:n.174-155G=
ENST00000562318.5:c.*362-155G= ENSP00000454395.1:n.*362-155G=
ENST00000565221.5:c.*258-155G= ENSP00000457932.1:n.*258-155G=
ENST00000566540.5:c.*262-155G= ENSP00000454284.1:n.*262-155G=
ENST00000566604.5:c.*180-155G= ENSP00000456774.1:n.*180-155G=
ENST00000566983.5:c.559-155G= ENSP00000457956.1:n.559-155G=
ENST00000567697.1:n.3808-155G=
ENST00000569958.5:c.367-155G= ENSP00000456302.1:n.367-155G=
ENST00000570076.5:c.*98-155G= ENSP00000456961.1:n.*98-155G=
NM_000303.2:c.640-155G= NP_000294.1:n.640-155G=
XM_005255374.3:c.391-155G= XP_005255431.1:n.391-155G=
XM_011522538.1:c.640-7465G= XP_011520840.1:n.640-7465G=
XM_005255374.4:c.391-155G= XP_005255431.1:n.391-155G=
NM_000303.3:c.640-155G= MANE Select NP_000294.1:n.640-155G=