Canonical Allele Identifier: CA2206132322

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8804787G= , CM000678.2:g.8804787G=	GRCh38
NC_000016.9:g.8898644G= , CM000678.1:g.8898644G=	GRCh37
NC_000016.8:g.8806145G=	NCBI36
NG_009209.1:g.11975G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682008.1:c.199G=	ENSP00000507849.1:p.Val67=
ENST00000682393.1:c.178+2877G=	ENSP00000506774.1:n.178+2877G=
ENST00000683094.1:c.179-1529G=	ENSP00000508230.1:n.179-1529G=
ENST00000683274.1:c.199G=	ENSP00000507262.1:p.Val67=
ENST00000683435.1:c.*195G=	ENSP00000508092.1:n.*195G=
ENST00000268261.9:c.199G= MANE Select	ENSP00000268261.4:p.Val67=
ENST00000268261.8:c.199G=	ENSP00000268261.4:p.Val67=
ENST00000562318.5:c.179-1529G=	ENSP00000454395.1:n.179-1529G=
ENST00000562448.1:n.220-1529G=
ENST00000564030.5:n.261G=
ENST00000564069.1:c.170G=
ENST00000565221.5:c.178+2877G=	ENSP00000457932.1:n.178+2877G=
ENST00000565896.5:c.*145+2398G=	ENSP00000456024.1:n.*145+2398G=
ENST00000566540.5:c.179-1529G=	ENSP00000454284.1:n.179-1529G=
ENST00000566604.5:c.199G=	ENSP00000456774.1:p.Val67=
ENST00000566983.5:c.118G=	ENSP00000457956.1:p.Val40=
ENST00000568602.5:c.*52G=	ENSP00000455066.1:n.*52G=
ENST00000569958.5:c.178+2877G=	ENSP00000456302.1:n.178+2877G=
ENST00000570076.5:c.178+2877G=	ENSP00000456961.1:n.178+2877G=
ENST00000570134.5:c.179-1529G=	ENSP00000456275.1:n.179-1529G=
NM_000303.2:c.199G=	NP_000294.1:p.Val67=
XM_005255372.3:c.199G=	XP_005255429.1:p.Val67=
XM_005255373.3:c.7-1529G=	XP_005255430.1:n.7-1529G=
XM_005255374.3:c.7-1529G=	XP_005255431.1:n.7-1529G=
XM_011522538.1:c.199G=	XP_011520840.1:p.Val67=
XM_011522539.1:c.-29+2877G=	XP_011520841.1:n.-29+2877G=
XM_005255374.4:c.7-1529G=	XP_005255431.1:n.7-1529G=
NM_000303.3:c.199G= MANE Select	NP_000294.1:p.Val67=