Canonical Allele Identifier: CA1724602

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461436C>T , CM000664.2:g.74461436C>T	GRCh38
NC_000002.11:g.74688563C>T , CM000664.1:g.74688563C>T	GRCh37
NC_000002.10:g.74542071C>T	NCBI36
NG_008922.1:g.8975G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.2059G>A	ENSP00000510501.1:p.Gly687Ser
ENST00000691308.1:c.1279G>A	ENSP00000509583.1:p.Gly427Ser
ENST00000448666.7:c.2353G>A MANE Select	ENSP00000410992.3:p.Gly785Ser
ENST00000452063.7:c.2035G>A	ENSP00000388201.2:p.Gly679Ser
ENST00000462443.2:c.1528G>A	ENSP00000497265.1:p.Gly510Ser
ENST00000647723.1:c.2296G>A
ENST00000647753.1:c.*1646G>A	ENSP00000497318.1:n.*1646G>A
ENST00000647771.1:c.*1841G>A	ENSP00000496788.1:n.*1841G>A
ENST00000647915.1:c.*1646G>A	ENSP00000498123.1:n.*1646G>A
ENST00000648768.1:n.2610G>A
ENST00000648810.1:c.1528G>A	ENSP00000496949.1:p.Gly510Ser
ENST00000649075.1:c.*1281G>A	ENSP00000497836.1:n.*1281G>A
ENST00000649601.1:c.*1533G>A	ENSP00000496796.1:n.*1533G>A
ENST00000649777.1:n.2562G>A
ENST00000649854.1:c.1986G>A
ENST00000233616.8:c.2353G>A	ENSP00000233616.4:p.Gly785Ser
ENST00000409065.5:c.*1533G>A	ENSP00000386493.1:n.*1533G>A
ENST00000452063.6:c.2035G>A	ENSP00000388201.2:p.Gly679Ser
ENST00000462189.1:n.2034G>A
NM_001146158.1:c.2035G>A	NP_001139630.1:p.Gly679Ser
NM_006302.2:c.2353G>A	NP_006293.2:p.Gly785Ser
NM_006302.3:c.2353G>A MANE Select	NP_006293.2:p.Gly785Ser
NM_001146158.2:c.2035G>A	NP_001139630.1:p.Gly679Ser