Canonical Allele Identifier: CA1724691

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461840C>T , CM000664.2:g.74461840C>T	GRCh38
NC_000002.11:g.74688967C>T , CM000664.1:g.74688967C>T	GRCh37
NC_000002.10:g.74542475C>T	NCBI36
NG_008922.1:g.8571G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1855+94G>A	ENSP00000510501.1:n.1855+94G>A
ENST00000691308.1:c.1075+94G>A	ENSP00000509583.1:n.1075+94G>A
ENST00000448666.7:c.1949G>A MANE Select	ENSP00000410992.3:p.Gly650Glu
ENST00000452063.7:c.1631G>A	ENSP00000388201.2:p.Gly544Glu
ENST00000462443.2:c.1124G>A	ENSP00000497265.1:p.Gly375Glu
ENST00000647723.1:c.1892G>A
ENST00000647753.1:c.*1242G>A	ENSP00000497318.1:n.*1242G>A
ENST00000647771.1:c.*1437G>A	ENSP00000496788.1:n.*1437G>A
ENST00000647915.1:c.*1242G>A	ENSP00000498123.1:n.*1242G>A
ENST00000648768.1:n.2206G>A
ENST00000648810.1:c.1124G>A	ENSP00000496949.1:p.Gly375Glu
ENST00000649075.1:c.*877G>A	ENSP00000497836.1:n.*877G>A
ENST00000649601.1:c.*1129G>A	ENSP00000496796.1:n.*1129G>A
ENST00000649777.1:n.2158G>A
ENST00000649854.1:c.1582G>A
ENST00000233616.8:c.1949G>A	ENSP00000233616.4:p.Gly650Glu
ENST00000409065.5:c.*1129G>A	ENSP00000386493.1:n.*1129G>A
ENST00000452063.6:c.1631G>A	ENSP00000388201.2:p.Gly544Glu
ENST00000462189.1:n.1630G>A
NM_001146158.1:c.1631G>A	NP_001139630.1:p.Gly544Glu
NM_006302.2:c.1949G>A	NP_006293.2:p.Gly650Glu
NM_006302.3:c.1949G>A MANE Select	NP_006293.2:p.Gly650Glu
NM_001146158.2:c.1631G>A	NP_001139630.1:p.Gly544Glu