Canonical Allele Identifier: CA7893838
Gene: PMM2 HGNC NCBI

Linked Data

dbSNP Id: rs771335903

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797859_8797863del , CM000678.2:g.8797859_8797863del GRCh38
NC_000016.9:g.8891716_8891720del , CM000678.1:g.8891716_8891720del GRCh37
NC_000016.8:g.8799217_8799221del NCBI36
NG_009209.1:g.5047_5051del
NG_033146.1:g.4788_4792del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682008.1:c.-24_-20del ENSP00000507849.1:n.-24_-20del
ENST00000682393.1:c.-24_-20del ENSP00000506774.1:n.-24_-20del
ENST00000683094.1:c.-24_-20del ENSP00000508230.1:n.-24_-20del
ENST00000683274.1:c.-24_-20del ENSP00000507262.1:n.-24_-20del
ENST00000683435.1:c.-24_-20del ENSP00000508092.1:n.-24_-20del
ENST00000268261.9:c.-24_-20del MANE Select ENSP00000268261.4:n.-24_-20del
ENST00000268261.8:c.-24_-20del ENSP00000268261.4:n.-24_-20del
ENST00000562318.5:c.-24_-20del ENSP00000454395.1:n.-24_-20del
ENST00000562448.1:n.18_22del
ENST00000564030.5:n.39_43del
ENST00000565896.5:c.-24_-20del ENSP00000456024.1:n.-24_-20del
ENST00000566196.5:n.21_25del
ENST00000566540.5:c.-24_-20del ENSP00000454284.1:n.-24_-20del
ENST00000566604.5:c.-24_-20del ENSP00000456774.1:n.-24_-20del
ENST00000566983.5:c.-15-3940_-15-3936del ENSP00000457956.1:n.-15-3940_-15-3936del
ENST00000568602.5:c.-24_-20del ENSP00000455066.1:n.-24_-20del
ENST00000570076.5:c.-24_-20del ENSP00000456961.1:n.-24_-20del
ENST00000570134.5:c.-24_-20del ENSP00000456275.1:n.-24_-20del
NM_000303.2:c.-24_-20del NP_000294.1:n.-24_-20del
XM_005255372.3:c.-24_-20del XP_005255429.1:n.-24_-20del
XM_005255373.3:c.-196_-192del XP_005255430.1:n.-196_-192del
XM_005255374.3:c.-196_-192del XP_005255431.1:n.-196_-192del
XM_011522538.1:c.-24_-20del XP_011520840.1:n.-24_-20del
XM_005255374.4:c.-196_-192del XP_005255431.1:n.-196_-192del
NM_000303.3:c.-24_-20del MANE Select NP_000294.1:n.-24_-20del