Canonical Allele Identifier: CA2206128247

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8797853T= , CM000678.2:g.8797853T=	GRCh38
NC_000016.9:g.8891710T= , CM000678.1:g.8891710T=	GRCh37
NC_000016.8:g.8799211T=	NCBI36
NG_009209.1:g.5041T=
NG_033146.1:g.4796A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682008.1:c.-30T=	ENSP00000507849.1:n.-30T=
ENST00000682393.1:c.-30T=	ENSP00000506774.1:n.-30T=
ENST00000683094.1:c.-30T=	ENSP00000508230.1:n.-30T=
ENST00000683274.1:c.-30T=	ENSP00000507262.1:n.-30T=
ENST00000683435.1:c.-30T=	ENSP00000508092.1:n.-30T=
ENST00000268261.9:c.-30T= MANE Select	ENSP00000268261.4:n.-30T=
ENST00000268261.8:c.-30T=	ENSP00000268261.4:n.-30T=
ENST00000562318.5:c.-30T=	ENSP00000454395.1:n.-30T=
ENST00000562448.1:n.12T=
ENST00000564030.5:n.33T=
ENST00000565896.5:c.-30T=	ENSP00000456024.1:n.-30T=
ENST00000566196.5:n.15T=
ENST00000566540.5:c.-30T=	ENSP00000454284.1:n.-30T=
ENST00000566604.5:c.-30T=	ENSP00000456774.1:n.-30T=
ENST00000566983.5:c.-15-3946T=	ENSP00000457956.1:n.-15-3946T=
ENST00000568602.5:c.-30T=	ENSP00000455066.1:n.-30T=
ENST00000570076.5:c.-30T=	ENSP00000456961.1:n.-30T=
ENST00000570134.5:c.-30T=	ENSP00000456275.1:n.-30T=
NM_000303.2:c.-30T=	NP_000294.1:n.-30T=
XM_005255372.3:c.-30T=	XP_005255429.1:n.-30T=
XM_005255373.3:c.-202T=	XP_005255430.1:n.-202T=
XM_005255374.3:c.-202T=	XP_005255431.1:n.-202T=
XM_011522538.1:c.-30T=	XP_011520840.1:n.-30T=
XM_005255374.4:c.-202T=	XP_005255431.1:n.-202T=
NM_000303.3:c.-30T= MANE Select	NP_000294.1:n.-30T=