Canonical Allele Identifier: CA1724694

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461845C>T , CM000664.2:g.74461845C>T	GRCh38
NC_000002.11:g.74688972C>T , CM000664.1:g.74688972C>T	GRCh37
NC_000002.10:g.74542480C>T	NCBI36
NG_008922.1:g.8566G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1855+89G>A	ENSP00000510501.1:n.1855+89G>A
ENST00000691308.1:c.1075+89G>A	ENSP00000509583.1:n.1075+89G>A
ENST00000448666.7:c.1944G>A MANE Select	ENSP00000410992.3:p.Glu648=
ENST00000452063.7:c.1626G>A	ENSP00000388201.2:p.Glu542=
ENST00000462443.2:c.1119G>A	ENSP00000497265.1:p.Glu373=
ENST00000647723.1:c.1887G>A
ENST00000647753.1:c.*1237G>A	ENSP00000497318.1:n.*1237G>A
ENST00000647771.1:c.*1432G>A	ENSP00000496788.1:n.*1432G>A
ENST00000647915.1:c.*1237G>A	ENSP00000498123.1:n.*1237G>A
ENST00000648768.1:n.2201G>A
ENST00000648810.1:c.1119G>A	ENSP00000496949.1:p.Glu373=
ENST00000649075.1:c.*872G>A	ENSP00000497836.1:n.*872G>A
ENST00000649601.1:c.*1124G>A	ENSP00000496796.1:n.*1124G>A
ENST00000649777.1:n.2153G>A
ENST00000649854.1:c.1577G>A
ENST00000233616.8:c.1944G>A	ENSP00000233616.4:p.Glu648=
ENST00000409065.5:c.*1124G>A	ENSP00000386493.1:n.*1124G>A
ENST00000452063.6:c.1626G>A	ENSP00000388201.2:p.Glu542=
ENST00000462189.1:n.1625G>A
NM_001146158.1:c.1626G>A	NP_001139630.1:p.Glu542=
NM_006302.2:c.1944G>A	NP_006293.2:p.Glu648=
NM_006302.3:c.1944G>A MANE Select	NP_006293.2:p.Glu648=
NM_001146158.2:c.1626G>A	NP_001139630.1:p.Glu542=