Canonical Allele Identifier: CA2206135653
Gene: PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8811018_8811019delinsTC , CM000678.2:g.8811018_8811019delinsTC GRCh38
NC_000016.9:g.8904875_8904876delinsTC , CM000678.1:g.8904875_8904876delinsTC GRCh37
NC_000016.8:g.8812376_8812377delinsTC NCBI36
NG_009209.1:g.18206_18207delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000567697.2:n.3455_3456delinsTC
ENST00000682008.1:c.348-61_348-60delinsTC ENSP00000507849.1:n.348-61_348-60delinsTC
ENST00000682393.1:c.179-61_179-60delinsTC ENSP00000506774.1:n.179-61_179-60delinsTC
ENST00000683094.1:c.*70-620_*70-619delinsTC ENSP00000508230.1:n.*70-620_*70-619delinsTC
ENST00000683274.1:c.348-620_348-619delinsTC ENSP00000507262.1:n.348-620_348-619delinsTC
ENST00000683435.1:c.*344-620_*344-619delinsTC ENSP00000508092.1:n.*344-620_*344-619delinsTC
ENST00000268261.9:c.348-61_348-60delinsTC MANE Select ENSP00000268261.4:n.348-61_348-60delinsTC
ENST00000268261.8:c.348-61_348-60delinsTC ENSP00000268261.4:n.348-61_348-60delinsTC
ENST00000562318.5:c.*70-61_*70-60delinsTC ENSP00000454395.1:n.*70-61_*70-60delinsTC
ENST00000564069.1:c.319-61_319-60delinsTC
ENST00000565221.5:c.179-61_179-60delinsTC ENSP00000457932.1:n.179-61_179-60delinsTC
ENST00000565896.5:c.*146-61_*146-60delinsTC ENSP00000456024.1:n.*146-61_*146-60delinsTC
ENST00000566540.5:c.*70-620_*70-619delinsTC ENSP00000454284.1:n.*70-620_*70-619delinsTC
ENST00000566604.5:c.348-620_348-619delinsTC ENSP00000456774.1:n.348-620_348-619delinsTC
ENST00000566983.5:c.267-61_267-60delinsTC ENSP00000457956.1:n.267-61_267-60delinsTC
ENST00000567697.1:n.3455_3456delinsTC
ENST00000568602.5:c.*201-61_*201-60delinsTC ENSP00000455066.1:n.*201-61_*201-60delinsTC
ENST00000569958.5:c.179-624_179-623delinsTC ENSP00000456302.1:n.179-624_179-623delinsTC
ENST00000570076.5:c.179-620_179-619delinsTC ENSP00000456961.1:n.179-620_179-619delinsTC
ENST00000570134.5:c.*70-620_*70-619delinsTC ENSP00000456275.1:n.*70-620_*70-619delinsTC
NM_000303.2:c.348-61_348-60delinsTC NP_000294.1:n.348-61_348-60delinsTC
XM_005255372.3:c.348-61_348-60delinsTC XP_005255429.1:n.348-61_348-60delinsTC
XM_005255373.3:c.99-61_99-60delinsTC XP_005255430.1:n.99-61_99-60delinsTC
XM_005255374.3:c.99-61_99-60delinsTC XP_005255431.1:n.99-61_99-60delinsTC
XM_011522538.1:c.348-61_348-60delinsTC XP_011520840.1:n.348-61_348-60delinsTC
XM_011522539.1:c.-28-61_-28-60delinsTC XP_011520841.1:n.-28-61_-28-60delinsTC
XM_005255374.4:c.99-61_99-60delinsTC XP_005255431.1:n.99-61_99-60delinsTC
NM_000303.3:c.348-61_348-60delinsTC MANE Select NP_000294.1:n.348-61_348-60delinsTC