Canonical Allele Identifier: CA620728853
Gene: PMM2 HGNC NCBI

Linked Data

dbSNP Id: rs1276642152

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8804702_8804705del , CM000678.2:g.8804702_8804705del GRCh38
NC_000016.9:g.8898559_8898562del , CM000678.1:g.8898559_8898562del GRCh37
NC_000016.8:g.8806060_8806063del NCBI36
NG_009209.1:g.11890_11893del

Transcript Alleles

HGVS Amino-acid change
ENST00000682008.1:c.179-65_179-62del ENSP00000507849.1:n.179-65_179-62del
ENST00000682393.1:c.178+2792_178+2795del ENSP00000506774.1:n.178+2792_178+2795del
ENST00000683094.1:c.179-1614_179-1611del ENSP00000508230.1:n.179-1614_179-1611del
ENST00000683274.1:c.179-65_179-62del ENSP00000507262.1:n.179-65_179-62del
ENST00000683435.1:c.*175-65_*175-62del ENSP00000508092.1:n.*175-65_*175-62del
ENST00000268261.9:c.179-65_179-62del MANE Select ENSP00000268261.4:n.179-65_179-62del
ENST00000268261.8:c.179-65_179-62del ENSP00000268261.4:n.179-65_179-62del
ENST00000562318.5:c.179-1614_179-1611del ENSP00000454395.1:n.179-1614_179-1611del
ENST00000562448.1:n.220-1614_220-1611del
ENST00000564030.5:n.241-65_241-62del
ENST00000564069.1:c.150-65_150-62del
ENST00000565221.5:c.178+2792_178+2795del ENSP00000457932.1:n.178+2792_178+2795del
ENST00000565896.5:c.*145+2313_*145+2316del ENSP00000456024.1:n.*145+2313_*145+2316de...
ENST00000566540.5:c.179-1614_179-1611del ENSP00000454284.1:n.179-1614_179-1611del
ENST00000566604.5:c.179-65_179-62del ENSP00000456774.1:n.179-65_179-62del
ENST00000566983.5:c.98-65_98-62del ENSP00000457956.1:n.98-65_98-62del
ENST00000568602.5:c.*32-65_*32-62del ENSP00000455066.1:n.*32-65_*32-62del
ENST00000569958.5:c.178+2792_178+2795del ENSP00000456302.1:n.178+2792_178+2795del
ENST00000570076.5:c.178+2792_178+2795del ENSP00000456961.1:n.178+2792_178+2795del
ENST00000570134.5:c.179-1614_179-1611del ENSP00000456275.1:n.179-1614_179-1611del
NM_000303.2:c.179-65_179-62del NP_000294.1:n.179-65_179-62del
XM_005255372.3:c.179-65_179-62del XP_005255429.1:n.179-65_179-62del
XM_005255373.3:c.7-1614_7-1611del XP_005255430.1:n.7-1614_7-1611del
XM_005255374.3:c.7-1614_7-1611del XP_005255431.1:n.7-1614_7-1611del
XM_011522538.1:c.179-65_179-62del XP_011520840.1:n.179-65_179-62del
XM_011522539.1:c.-29+2792_-29+2795del XP_011520841.1:n.-29+2792_-29+2795del
XM_005255374.4:c.7-1614_7-1611del XP_005255431.1:n.7-1614_7-1611del
NM_000303.3:c.179-65_179-62del MANE Select NP_000294.1:n.179-65_179-62del