Canonical Allele Identifier: CA7893895

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8801856G>A , CM000678.2:g.8801856G>A	GRCh38
NC_000016.9:g.8895713G>A , CM000678.1:g.8895713G>A	GRCh37
NC_000016.8:g.8803214G>A	NCBI36
NG_009209.1:g.9044G>A
NG_033146.1:g.793C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682008.1:c.124G>A	ENSP00000507849.1:p.Gly42Arg
ENST00000682393.1:c.124G>A	ENSP00000506774.1:p.Gly42Arg
ENST00000683094.1:c.124G>A	ENSP00000508230.1:p.Gly42Arg
ENST00000683274.1:c.124G>A	ENSP00000507262.1:p.Gly42Arg
ENST00000683435.1:c.124G>A	ENSP00000508092.1:p.Gly42Arg
ENST00000268261.9:c.124G>A MANE Select	ENSP00000268261.4:p.Gly42Arg
ENST00000268261.8:c.124G>A	ENSP00000268261.4:p.Gly42Arg
ENST00000562318.5:c.124G>A	ENSP00000454395.1:p.Gly42Arg
ENST00000562448.1:n.165G>A
ENST00000564030.5:n.186G>A
ENST00000564069.1:c.95G>A
ENST00000565221.5:c.124G>A	ENSP00000457932.1:p.Gly42Arg
ENST00000565896.5:c.124G>A	ENSP00000456024.1:p.Gly42Arg
ENST00000566196.5:n.168G>A
ENST00000566540.5:c.124G>A	ENSP00000454284.1:p.Gly42Arg
ENST00000566604.5:c.124G>A	ENSP00000456774.1:p.Gly42Arg
ENST00000566983.5:c.43G>A	ENSP00000457956.1:p.Gly15Arg
ENST00000568602.5:c.124G>A	ENSP00000455066.1:p.Gly42Arg
ENST00000569958.5:c.124G>A	ENSP00000456302.1:p.Gly42Arg
ENST00000570076.5:c.124G>A	ENSP00000456961.1:p.Gly42Arg
ENST00000570134.5:c.124G>A	ENSP00000456275.1:p.Gly42Arg
NM_000303.2:c.124G>A	NP_000294.1:p.Gly42Arg
XM_005255372.3:c.124G>A	XP_005255429.1:p.Gly42Arg
XM_005255373.3:c.-49G>A	XP_005255430.1:n.-49G>A
XM_005255374.3:c.-49G>A	XP_005255431.1:n.-49G>A
XM_011522538.1:c.124G>A	XP_011520840.1:p.Gly42Arg
XM_011522539.1:c.-83G>A	XP_011520841.1:n.-83G>A
XM_005255374.4:c.-49G>A	XP_005255431.1:n.-49G>A
NM_000303.3:c.124G>A MANE Select	NP_000294.1:p.Gly42Arg