Canonical Allele Identifier: CA2206158145

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8847867A= , CM000678.2:g.8847867A=	GRCh38
NC_000016.9:g.8941724A= , CM000678.1:g.8941724A=	GRCh37
NC_000016.8:g.8849225A=	NCBI36
NG_009209.1:g.55055A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.3951A=
ENST00000682393.1:c.*258-1502A=	ENSP00000506774.1:n.*258-1502A=
ENST00000683094.1:c.*262-1502A=	ENSP00000508230.1:n.*262-1502A=
ENST00000683274.1:c.*180-1502A=	ENSP00000507262.1:n.*180-1502A=
ENST00000683435.1:c.*679A=	ENSP00000508092.1:n.*679A=
ENST00000268261.9:c.*42A= MANE Select	ENSP00000268261.4:n.*42A=
ENST00000268261.8:c.*42A=	ENSP00000268261.4:n.*42A=
ENST00000562025.1:n.317A=
ENST00000562318.5:c.*505A=	ENSP00000454395.1:n.*505A=
ENST00000565221.5:c.*401A=	ENSP00000457932.1:n.*401A=
ENST00000566540.5:c.*405A=	ENSP00000454284.1:n.*405A=
ENST00000566604.5:c.*323A=	ENSP00000456774.1:n.*323A=
ENST00000566983.5:c.*42A=	ENSP00000457956.1:n.*42A=
ENST00000567697.1:n.3951A=
ENST00000569958.5:c.*42A=	ENSP00000456302.1:n.*42A=
ENST00000570076.5:c.*241A=	ENSP00000456961.1:n.*241A=
NM_000303.2:c.*42A=	NP_000294.1:n.*42A=
XM_005255374.3:c.*42A=	XP_005255431.1:n.*42A=
XM_011522538.1:c.640-7167A=	XP_011520840.1:n.640-7167A=
XM_005255374.4:c.*42A=	XP_005255431.1:n.*42A=
NM_000303.3:c.*42A= MANE Select	NP_000294.1:n.*42A=