Canonical Allele Identifier: CA2206136753

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8813090G= , CM000678.2:g.8813090G=	GRCh38
NC_000016.9:g.8906947G= , CM000678.1:g.8906947G=	GRCh37
NC_000016.8:g.8814448G=	NCBI36
NG_009209.1:g.20278G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000303.3:c.623G= MANE Select	NP_000294.1:p.Gly208=
ENST00000268261.9:c.623G= MANE Select	ENSP00000268261.4:p.Gly208=
NM_000303.2:c.623G=	NP_000294.1:p.Gly208=
ENST00000268261.8:c.623G=	ENSP00000268261.4:p.Gly208=
ENST00000562318.5:c.*345G=	ENSP00000454395.1:n.*345G=
ENST00000565221.5:c.*241G=	ENSP00000457932.1:n.*241G=
ENST00000566540.5:c.*245G=	ENSP00000454284.1:n.*245G=
ENST00000566604.5:c.*163G=	ENSP00000456774.1:n.*163G=
ENST00000566983.5:c.542G=	ENSP00000457956.1:p.Gly181=
ENST00000567697.1:n.3791G=
ENST00000567697.2:n.3791G=
ENST00000569958.5:c.350G=	ENSP00000456302.1:p.Gly117=
ENST00000570076.5:c.*81G=	ENSP00000456961.1:n.*81G=
ENST00000570134.5:c.*245G=	ENSP00000456275.1:n.*245G=
ENST00000682008.1:c.623G=	ENSP00000507849.1:p.Gly208=
ENST00000682393.1:c.*241G=	ENSP00000506774.1:n.*241G=
ENST00000683094.1:c.*245G=	ENSP00000508230.1:n.*245G=
ENST00000683274.1:c.*163G=	ENSP00000507262.1:n.*163G=
ENST00000683435.1:c.*519G=	ENSP00000508092.1:n.*519G=
XM_005255372.3:c.623G=	XP_005255429.1:p.Gly208=
XM_005255373.3:c.374G=	XP_005255430.1:p.Gly125=
XM_005255374.3:c.374G=	XP_005255431.1:p.Gly125=
XM_005255374.4:c.374G=	XP_005255431.1:p.Gly125=
XM_011522538.1:c.623G=	XP_011520840.1:p.Gly208=
XM_011522539.1:c.248G=	XP_011520841.1:p.Gly83=