Canonical Allele Identifier: CA2206158314

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8848086A= , CM000678.2:g.8848086A=	GRCh38
NC_000016.9:g.8941943A= , CM000678.1:g.8941943A=	GRCh37
NC_000016.8:g.8849444A=	NCBI36
NG_009209.1:g.55274A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.4170A=
ENST00000682393.1:c.*258-1283A=	ENSP00000506774.1:n.*258-1283A=
ENST00000683094.1:c.*262-1283A=	ENSP00000508230.1:n.*262-1283A=
ENST00000683274.1:c.*180-1283A=	ENSP00000507262.1:n.*180-1283A=
ENST00000268261.9:c.*261A= MANE Select	ENSP00000268261.4:n.*261A=
ENST00000268261.8:c.*261A=	ENSP00000268261.4:n.*261A=
ENST00000562025.1:n.536A=
ENST00000566540.5:c.*624A=	ENSP00000454284.1:n.*624A=
ENST00000566604.5:c.*542A=	ENSP00000456774.1:n.*542A=
ENST00000567697.1:n.4170A=
ENST00000570076.5:c.*460A=	ENSP00000456961.1:n.*460A=
NM_000303.2:c.*261A=	NP_000294.1:n.*261A=
XM_005255374.3:c.*261A=	XP_005255431.1:n.*261A=
XM_011522538.1:c.640-6948A=	XP_011520840.1:n.640-6948A=
XM_005255374.4:c.*261A=	XP_005255431.1:n.*261A=
NM_000303.3:c.*261A= MANE Select	NP_000294.1:n.*261A=