Canonical Allele Identifier: CA2206132219

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8804609_8804612delinsCTTT , CM000678.2:g.8804609_8804612delinsCTTT	GRCh38
NC_000016.9:g.8898466_8898469delinsCTTT , CM000678.1:g.8898466_8898469delinsCTTT	GRCh37
NC_000016.8:g.8805967_8805970delinsCTTT	NCBI36
NG_009209.1:g.11797_11800delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682008.1:c.179-158_179-155delinsCTTT	ENSP00000507849.1:n.179-158_179-155delinsCTTT
ENST00000682393.1:c.178+2699_178+2702delinsCTTT	ENSP00000506774.1:n.178+2699_178+2702delinsCTTT
ENST00000683094.1:c.179-1707_179-1704delinsCTTT	ENSP00000508230.1:n.179-1707_179-1704delinsCTTT
ENST00000683274.1:c.179-158_179-155delinsCTTT	ENSP00000507262.1:n.179-158_179-155delinsCTTT
ENST00000683435.1:c.*175-158_*175-155delinsCTTT	ENSP00000508092.1:n.*175-158_*175-155delinsCTTT
ENST00000268261.9:c.179-158_179-155delinsCTTT MANE Select	ENSP00000268261.4:n.179-158_179-155delinsCTTT
ENST00000268261.8:c.179-158_179-155delinsCTTT	ENSP00000268261.4:n.179-158_179-155delinsCTTT
ENST00000562318.5:c.179-1707_179-1704delinsCTTT	ENSP00000454395.1:n.179-1707_179-1704delinsCTTT
ENST00000562448.1:n.220-1707_220-1704delinsCTTT
ENST00000564030.5:n.241-158_241-155delinsCTTT
ENST00000564069.1:c.150-158_150-155delinsCTTT
ENST00000565221.5:c.178+2699_178+2702delinsCTTT	ENSP00000457932.1:n.178+2699_178+2702delinsCTTT
ENST00000565896.5:c.*145+2220_*145+2223delinsCTTT	ENSP00000456024.1:n.*145+2220_*145+2223delinsCTTT
ENST00000566540.5:c.179-1707_179-1704delinsCTTT	ENSP00000454284.1:n.179-1707_179-1704delinsCTTT
ENST00000566604.5:c.179-158_179-155delinsCTTT	ENSP00000456774.1:n.179-158_179-155delinsCTTT
ENST00000566983.5:c.98-158_98-155delinsCTTT	ENSP00000457956.1:n.98-158_98-155delinsCTTT
ENST00000568602.5:c.*32-158_*32-155delinsCTTT	ENSP00000455066.1:n.*32-158_*32-155delinsCTTT
ENST00000569958.5:c.178+2699_178+2702delinsCTTT	ENSP00000456302.1:n.178+2699_178+2702delinsCTTT
ENST00000570076.5:c.178+2699_178+2702delinsCTTT	ENSP00000456961.1:n.178+2699_178+2702delinsCTTT
ENST00000570134.5:c.179-1707_179-1704delinsCTTT	ENSP00000456275.1:n.179-1707_179-1704delinsCTTT
NM_000303.2:c.179-158_179-155delinsCTTT	NP_000294.1:n.179-158_179-155delinsCTTT
XM_005255372.3:c.179-158_179-155delinsCTTT	XP_005255429.1:n.179-158_179-155delinsCTTT
XM_005255373.3:c.7-1707_7-1704delinsCTTT	XP_005255430.1:n.7-1707_7-1704delinsCTTT
XM_005255374.3:c.7-1707_7-1704delinsCTTT	XP_005255431.1:n.7-1707_7-1704delinsCTTT
XM_011522538.1:c.179-158_179-155delinsCTTT	XP_011520840.1:n.179-158_179-155delinsCTTT
XM_011522539.1:c.-29+2699_-29+2702delinsCTTT	XP_011520841.1:n.-29+2699_-29+2702delinsCTTT
XM_005255374.4:c.7-1707_7-1704delinsCTTT	XP_005255431.1:n.7-1707_7-1704delinsCTTT
NM_000303.3:c.179-158_179-155delinsCTTT MANE Select	NP_000294.1:n.179-158_179-155delinsCTTT