Canonical Allele Identifier: CA725526392
Gene: PMM2 HGNC NCBI

Linked Data

dbSNP Id: rs141896135
gnomAD v4: 16-8804693-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8804693C>A , CM000678.2:g.8804693C>A GRCh38
NC_000016.9:g.8898550C>A , CM000678.1:g.8898550C>A GRCh37
NC_000016.8:g.8806051C>A NCBI36
NG_009209.1:g.11881C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682008.1:c.179-74C>A ENSP00000507849.1:n.179-74C>A
ENST00000682393.1:c.178+2783C>A ENSP00000506774.1:n.178+2783C>A
ENST00000683094.1:c.179-1623C>A ENSP00000508230.1:n.179-1623C>A
ENST00000683274.1:c.179-74C>A ENSP00000507262.1:n.179-74C>A
ENST00000683435.1:c.*175-74C>A ENSP00000508092.1:n.*175-74C>A
ENST00000268261.9:c.179-74C>A MANE Select ENSP00000268261.4:n.179-74C>A
ENST00000268261.8:c.179-74C>A ENSP00000268261.4:n.179-74C>A
ENST00000562318.5:c.179-1623C>A ENSP00000454395.1:n.179-1623C>A
ENST00000562448.1:n.220-1623C>A
ENST00000564030.5:n.241-74C>A
ENST00000564069.1:c.150-74C>A
ENST00000565221.5:c.178+2783C>A ENSP00000457932.1:n.178+2783C>A
ENST00000565896.5:c.*145+2304C>A ENSP00000456024.1:n.*145+2304C>A
ENST00000566540.5:c.179-1623C>A ENSP00000454284.1:n.179-1623C>A
ENST00000566604.5:c.179-74C>A ENSP00000456774.1:n.179-74C>A
ENST00000566983.5:c.98-74C>A ENSP00000457956.1:n.98-74C>A
ENST00000568602.5:c.*32-74C>A ENSP00000455066.1:n.*32-74C>A
ENST00000569958.5:c.178+2783C>A ENSP00000456302.1:n.178+2783C>A
ENST00000570076.5:c.178+2783C>A ENSP00000456961.1:n.178+2783C>A
ENST00000570134.5:c.179-1623C>A ENSP00000456275.1:n.179-1623C>A
NM_000303.2:c.179-74C>A NP_000294.1:n.179-74C>A
XM_005255372.3:c.179-74C>A XP_005255429.1:n.179-74C>A
XM_005255373.3:c.7-1623C>A XP_005255430.1:n.7-1623C>A
XM_005255374.3:c.7-1623C>A XP_005255431.1:n.7-1623C>A
XM_011522538.1:c.179-74C>A XP_011520840.1:n.179-74C>A
XM_011522539.1:c.-29+2783C>A XP_011520841.1:n.-29+2783C>A
XM_005255374.4:c.7-1623C>A XP_005255431.1:n.7-1623C>A
NM_000303.3:c.179-74C>A MANE Select NP_000294.1:n.179-74C>A