Canonical Allele Identifier: CA2206132346

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8804836G= , CM000678.2:g.8804836G=	GRCh38
NC_000016.9:g.8898693G= , CM000678.1:g.8898693G=	GRCh37
NC_000016.8:g.8806194G=	NCBI36
NG_009209.1:g.12024G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682008.1:c.248G=	ENSP00000507849.1:p.Cys83=
ENST00000682393.1:c.178+2926G=	ENSP00000506774.1:n.178+2926G=
ENST00000683094.1:c.179-1480G=	ENSP00000508230.1:n.179-1480G=
ENST00000683274.1:c.248G=	ENSP00000507262.1:p.Cys83=
ENST00000683435.1:c.*244G=	ENSP00000508092.1:n.*244G=
ENST00000268261.9:c.248G= MANE Select	ENSP00000268261.4:p.Cys83=
ENST00000268261.8:c.248G=	ENSP00000268261.4:p.Cys83=
ENST00000562318.5:c.179-1480G=	ENSP00000454395.1:n.179-1480G=
ENST00000562448.1:n.220-1480G=
ENST00000564030.5:n.310G=
ENST00000564069.1:c.219G=
ENST00000565221.5:c.178+2926G=	ENSP00000457932.1:n.178+2926G=
ENST00000565896.5:c.*145+2447G=	ENSP00000456024.1:n.*145+2447G=
ENST00000566540.5:c.179-1480G=	ENSP00000454284.1:n.179-1480G=
ENST00000566604.5:c.248G=	ENSP00000456774.1:p.Cys83=
ENST00000566983.5:c.167G=	ENSP00000457956.1:p.Cys56=
ENST00000568602.5:c.*101G=	ENSP00000455066.1:n.*101G=
ENST00000569958.5:c.178+2926G=	ENSP00000456302.1:n.178+2926G=
ENST00000570076.5:c.178+2926G=	ENSP00000456961.1:n.178+2926G=
ENST00000570134.5:c.179-1480G=	ENSP00000456275.1:n.179-1480G=
NM_000303.2:c.248G=	NP_000294.1:p.Cys83=
XM_005255372.3:c.248G=	XP_005255429.1:p.Cys83=
XM_005255373.3:c.7-1480G=	XP_005255430.1:n.7-1480G=
XM_005255374.3:c.7-1480G=	XP_005255431.1:n.7-1480G=
XM_011522538.1:c.248G=	XP_011520840.1:p.Cys83=
XM_011522539.1:c.-29+2926G=	XP_011520841.1:n.-29+2926G=
XM_005255374.4:c.7-1480G=	XP_005255431.1:n.7-1480G=
NM_000303.3:c.248G= MANE Select	NP_000294.1:p.Cys83=