Canonical Allele Identifier: CA7894038

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8811097C>T , CM000678.2:g.8811097C>T	GRCh38
NC_000016.9:g.8904954C>T , CM000678.1:g.8904954C>T	GRCh37
NC_000016.8:g.8812455C>T	NCBI36
NG_009209.1:g.18285C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.3534C>T
ENST00000682008.1:c.366C>T	ENSP00000507849.1:p.Phe122=
ENST00000682393.1:c.197C>T	ENSP00000506774.1:p.Ser66Phe
ENST00000683094.1:c.*70-541C>T	ENSP00000508230.1:n.*70-541C>T
ENST00000683274.1:c.348-541C>T	ENSP00000507262.1:n.348-541C>T
ENST00000683435.1:c.*344-541C>T	ENSP00000508092.1:n.*344-541C>T
ENST00000268261.9:c.366C>T MANE Select	ENSP00000268261.4:p.Phe122=
ENST00000268261.8:c.366C>T	ENSP00000268261.4:p.Phe122=
ENST00000562318.5:c.*88C>T	ENSP00000454395.1:n.*88C>T
ENST00000564069.1:c.337C>T
ENST00000565221.5:c.197C>T	ENSP00000457932.1:p.Ser66Phe
ENST00000565896.5:c.*164C>T	ENSP00000456024.1:n.*164C>T
ENST00000566540.5:c.*70-541C>T	ENSP00000454284.1:n.*70-541C>T
ENST00000566604.5:c.348-541C>T	ENSP00000456774.1:n.348-541C>T
ENST00000566983.5:c.285C>T	ENSP00000457956.1:p.Phe95=
ENST00000567697.1:n.3534C>T
ENST00000568602.5:c.*219C>T	ENSP00000455066.1:n.*219C>T
ENST00000569958.5:c.179-545C>T	ENSP00000456302.1:n.179-545C>T
ENST00000570076.5:c.179-541C>T	ENSP00000456961.1:n.179-541C>T
ENST00000570134.5:c.*70-541C>T	ENSP00000456275.1:n.*70-541C>T
NM_000303.2:c.366C>T	NP_000294.1:p.Phe122=
XM_005255372.3:c.366C>T	XP_005255429.1:p.Phe122=
XM_005255373.3:c.117C>T	XP_005255430.1:p.Phe39=
XM_005255374.3:c.117C>T	XP_005255431.1:p.Phe39=
XM_011522538.1:c.366C>T	XP_011520840.1:p.Phe122=
XM_011522539.1:c.-10C>T	XP_011520841.1:n.-10C>T
XM_005255374.4:c.117C>T	XP_005255431.1:p.Phe39=
NM_000303.3:c.366C>T MANE Select	NP_000294.1:p.Phe122=