Canonical Allele Identifier: CA2731682963

Gene: PMM2

Linked Data

• dbSNP Id: rs2141022887

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8811023_8811024insCTG , CM000678.2:g.8811023_8811024insCTG	GRCh38
NC_000016.9:g.8904880_8904881insCTG , CM000678.1:g.8904880_8904881insCTG	GRCh37
NC_000016.8:g.8812381_8812382insCTG	NCBI36
NG_009209.1:g.18211_18212insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.3460_3461insCTG
ENST00000682008.1:c.348-56_348-55insCTG	ENSP00000507849.1:n.348-56_348-55insCTG
ENST00000682393.1:c.179-56_179-55insCTG	ENSP00000506774.1:n.179-56_179-55insCTG
ENST00000683094.1:c.*70-615_*70-614insCTG	ENSP00000508230.1:n.*70-615_*70-614insCTG
ENST00000683274.1:c.348-615_348-614insCTG	ENSP00000507262.1:n.348-615_348-614insCTG
ENST00000683435.1:c.*344-615_*344-614insCTG	ENSP00000508092.1:n.*344-615_*344-614insCTG
ENST00000268261.9:c.348-56_348-55insCTG MANE Select	ENSP00000268261.4:n.348-56_348-55insCTG
ENST00000268261.8:c.348-56_348-55insCTG	ENSP00000268261.4:n.348-56_348-55insCTG
ENST00000562318.5:c.*70-56_*70-55insCTG	ENSP00000454395.1:n.*70-56_*70-55insCTG
ENST00000564069.1:c.319-56_319-55insCTG
ENST00000565221.5:c.179-56_179-55insCTG	ENSP00000457932.1:n.179-56_179-55insCTG
ENST00000565896.5:c.*146-56_*146-55insCTG	ENSP00000456024.1:n.*146-56_*146-55insCTG
ENST00000566540.5:c.*70-615_*70-614insCTG	ENSP00000454284.1:n.*70-615_*70-614insCTG
ENST00000566604.5:c.348-615_348-614insCTG	ENSP00000456774.1:n.348-615_348-614insCTG
ENST00000566983.5:c.267-56_267-55insCTG	ENSP00000457956.1:n.267-56_267-55insCTG
ENST00000567697.1:n.3460_3461insCTG
ENST00000568602.5:c.*201-56_*201-55insCTG	ENSP00000455066.1:n.*201-56_*201-55insCTG
ENST00000569958.5:c.179-619_179-618insCTG	ENSP00000456302.1:n.179-619_179-618insCTG
ENST00000570076.5:c.179-615_179-614insCTG	ENSP00000456961.1:n.179-615_179-614insCTG
ENST00000570134.5:c.*70-615_*70-614insCTG	ENSP00000456275.1:n.*70-615_*70-614insCTG
NM_000303.2:c.348-56_348-55insCTG	NP_000294.1:n.348-56_348-55insCTG
XM_005255372.3:c.348-56_348-55insCTG	XP_005255429.1:n.348-56_348-55insCTG
XM_005255373.3:c.99-56_99-55insCTG	XP_005255430.1:n.99-56_99-55insCTG
XM_005255374.3:c.99-56_99-55insCTG	XP_005255431.1:n.99-56_99-55insCTG
XM_011522538.1:c.348-56_348-55insCTG	XP_011520840.1:n.348-56_348-55insCTG
XM_011522539.1:c.-28-56_-28-55insCTG	XP_011520841.1:n.-28-56_-28-55insCTG
XM_005255374.4:c.99-56_99-55insCTG	XP_005255431.1:n.99-56_99-55insCTG
NM_000303.3:c.348-56_348-55insCTG MANE Select	NP_000294.1:n.348-56_348-55insCTG