Canonical Allele Identifier: CA2206157958
Gene: PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8847576T= , CM000678.2:g.8847576T= GRCh38
NC_000016.9:g.8941433T= , CM000678.1:g.8941433T= GRCh37
NC_000016.8:g.8848934T= NCBI36
NG_009209.1:g.54764T=

Transcript Alleles

HGVS Amino-acid change
ENST00000567697.2:n.3808-148T=
ENST00000682393.1:c.*258-1793T= ENSP00000506774.1:n.*258-1793T=
ENST00000683094.1:c.*262-1793T= ENSP00000508230.1:n.*262-1793T=
ENST00000683274.1:c.*180-1793T= ENSP00000507262.1:n.*180-1793T=
ENST00000683435.1:c.*536-148T= ENSP00000508092.1:n.*536-148T=
ENST00000268261.9:c.640-148T= MANE Select ENSP00000268261.4:n.640-148T=
ENST00000268261.8:c.640-148T= ENSP00000268261.4:n.640-148T=
ENST00000562025.1:n.174-148T=
ENST00000562318.5:c.*362-148T= ENSP00000454395.1:n.*362-148T=
ENST00000565221.5:c.*258-148T= ENSP00000457932.1:n.*258-148T=
ENST00000566540.5:c.*262-148T= ENSP00000454284.1:n.*262-148T=
ENST00000566604.5:c.*180-148T= ENSP00000456774.1:n.*180-148T=
ENST00000566983.5:c.559-148T= ENSP00000457956.1:n.559-148T=
ENST00000567697.1:n.3808-148T=
ENST00000569958.5:c.367-148T= ENSP00000456302.1:n.367-148T=
ENST00000570076.5:c.*98-148T= ENSP00000456961.1:n.*98-148T=
NM_000303.2:c.640-148T= NP_000294.1:n.640-148T=
XM_005255374.3:c.391-148T= XP_005255431.1:n.391-148T=
XM_011522538.1:c.640-7458T= XP_011520840.1:n.640-7458T=
XM_005255374.4:c.391-148T= XP_005255431.1:n.391-148T=
NM_000303.3:c.640-148T= MANE Select NP_000294.1:n.640-148T=