Canonical Allele Identifier: CA347367379

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461632G>T , CM000664.2:g.74461632G>T	GRCh38
NC_000002.11:g.74688759G>T , CM000664.1:g.74688759G>T	GRCh37
NC_000002.10:g.74542267G>T	NCBI36
NG_008922.1:g.8779C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1863C>A	ENSP00000510501.1:p.Ser621Arg
ENST00000691308.1:c.1083C>A	ENSP00000509583.1:p.Ser361Arg
ENST00000448666.7:c.2157C>A MANE Select	ENSP00000410992.3:p.Ser719Arg
ENST00000452063.7:c.1839C>A	ENSP00000388201.2:p.Ser613Arg
ENST00000462443.2:c.1332C>A	ENSP00000497265.1:p.Ser444Arg
ENST00000647723.1:c.2100C>A
ENST00000647753.1:c.*1450C>A	ENSP00000497318.1:n.*1450C>A
ENST00000647771.1:c.*1645C>A	ENSP00000496788.1:n.*1645C>A
ENST00000647915.1:c.*1450C>A	ENSP00000498123.1:n.*1450C>A
ENST00000648768.1:n.2414C>A
ENST00000648810.1:c.1332C>A	ENSP00000496949.1:p.Ser444Arg
ENST00000649075.1:c.*1085C>A	ENSP00000497836.1:n.*1085C>A
ENST00000649601.1:c.*1337C>A	ENSP00000496796.1:n.*1337C>A
ENST00000649777.1:n.2366C>A
ENST00000649854.1:c.1790C>A
ENST00000233616.8:c.2157C>A	ENSP00000233616.4:p.Ser719Arg
ENST00000409065.5:c.*1337C>A	ENSP00000386493.1:n.*1337C>A
ENST00000452063.6:c.1839C>A	ENSP00000388201.2:p.Ser613Arg
ENST00000462189.1:n.1838C>A
NM_001146158.1:c.1839C>A	NP_001139630.1:p.Ser613Arg
NM_006302.2:c.2157C>A	NP_006293.2:p.Ser719Arg
NM_006302.3:c.2157C>A MANE Select	NP_006293.2:p.Ser719Arg
NM_001146158.2:c.1839C>A	NP_001139630.1:p.Ser613Arg