Canonical Allele Identifier: CA2206135699

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8811095T= , CM000678.2:g.8811095T=	GRCh38
NC_000016.9:g.8904952T= , CM000678.1:g.8904952T=	GRCh37
NC_000016.8:g.8812453T=	NCBI36
NG_009209.1:g.18283T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.3532T=
ENST00000682008.1:c.364T=	ENSP00000507849.1:p.Phe122=
ENST00000682393.1:c.195T=	ENSP00000506774.1:p.Asn65=
ENST00000683094.1:c.*70-543T=	ENSP00000508230.1:n.*70-543T=
ENST00000683274.1:c.348-543T=	ENSP00000507262.1:n.348-543T=
ENST00000683435.1:c.*344-543T=	ENSP00000508092.1:n.*344-543T=
ENST00000268261.9:c.364T= MANE Select	ENSP00000268261.4:p.Phe122=
ENST00000268261.8:c.364T=	ENSP00000268261.4:p.Phe122=
ENST00000562318.5:c.*86T=	ENSP00000454395.1:n.*86T=
ENST00000564069.1:c.335T=
ENST00000565221.5:c.195T=	ENSP00000457932.1:p.Asn65=
ENST00000565896.5:c.*162T=	ENSP00000456024.1:n.*162T=
ENST00000566540.5:c.*70-543T=	ENSP00000454284.1:n.*70-543T=
ENST00000566604.5:c.348-543T=	ENSP00000456774.1:n.348-543T=
ENST00000566983.5:c.283T=	ENSP00000457956.1:p.Phe95=
ENST00000567697.1:n.3532T=
ENST00000568602.5:c.*217T=	ENSP00000455066.1:n.*217T=
ENST00000569958.5:c.179-547T=	ENSP00000456302.1:n.179-547T=
ENST00000570076.5:c.179-543T=	ENSP00000456961.1:n.179-543T=
ENST00000570134.5:c.*70-543T=	ENSP00000456275.1:n.*70-543T=
NM_000303.2:c.364T=	NP_000294.1:p.Phe122=
XM_005255372.3:c.364T=	XP_005255429.1:p.Phe122=
XM_005255373.3:c.115T=	XP_005255430.1:p.Phe39=
XM_005255374.3:c.115T=	XP_005255431.1:p.Phe39=
XM_011522538.1:c.364T=	XP_011520840.1:p.Phe122=
XM_011522539.1:c.-12T=	XP_011520841.1:n.-12T=
XM_005255374.4:c.115T=	XP_005255431.1:p.Phe39=
NM_000303.3:c.364T= MANE Select	NP_000294.1:p.Phe122=