Canonical Allele Identifier: CA394696517

Gene: PMM2

Linked Data

• MyVariant Identifiers: chr16:g.8904949G>C (hg19) ; chr16:g.8811092G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8811092G>C , CM000678.2:g.8811092G>C	GRCh38
NC_000016.9:g.8904949G>C , CM000678.1:g.8904949G>C	GRCh37
NC_000016.8:g.8812450G>C	NCBI36
NG_009209.1:g.18280G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.3529G>C
ENST00000682008.1:c.361G>C	ENSP00000507849.1:p.Glu121Gln
ENST00000682393.1:c.192G>C	ENSP00000506774.1:p.Leu64Phe
ENST00000683094.1:c.*70-546G>C	ENSP00000508230.1:n.*70-546G>C
ENST00000683274.1:c.348-546G>C	ENSP00000507262.1:n.348-546G>C
ENST00000683435.1:c.*344-546G>C	ENSP00000508092.1:n.*344-546G>C
ENST00000268261.9:c.361G>C MANE Select	ENSP00000268261.4:p.Glu121Gln
ENST00000268261.8:c.361G>C	ENSP00000268261.4:p.Glu121Gln
ENST00000562318.5:c.*83G>C	ENSP00000454395.1:n.*83G>C
ENST00000564069.1:c.332G>C
ENST00000565221.5:c.192G>C	ENSP00000457932.1:p.Leu64Phe
ENST00000565896.5:c.*159G>C	ENSP00000456024.1:n.*159G>C
ENST00000566540.5:c.*70-546G>C	ENSP00000454284.1:n.*70-546G>C
ENST00000566604.5:c.348-546G>C	ENSP00000456774.1:n.348-546G>C
ENST00000566983.5:c.280G>C	ENSP00000457956.1:p.Glu94Gln
ENST00000567697.1:n.3529G>C
ENST00000568602.5:c.*214G>C	ENSP00000455066.1:n.*214G>C
ENST00000569958.5:c.179-550G>C	ENSP00000456302.1:n.179-550G>C
ENST00000570076.5:c.179-546G>C	ENSP00000456961.1:n.179-546G>C
ENST00000570134.5:c.*70-546G>C	ENSP00000456275.1:n.*70-546G>C
NM_000303.2:c.361G>C	NP_000294.1:p.Glu121Gln
XM_005255372.3:c.361G>C	XP_005255429.1:p.Glu121Gln
XM_005255373.3:c.112G>C	XP_005255430.1:p.Glu38Gln
XM_005255374.3:c.112G>C	XP_005255431.1:p.Glu38Gln
XM_011522538.1:c.361G>C	XP_011520840.1:p.Glu121Gln
XM_011522539.1:c.-15G>C	XP_011520841.1:n.-15G>C
XM_005255374.4:c.112G>C	XP_005255431.1:p.Glu38Gln
NM_000303.3:c.361G>C MANE Select	NP_000294.1:p.Glu121Gln