Canonical Allele Identifier: CA1261438268

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462332C= , CM000664.2:g.74462332C=	GRCh38
NC_000002.11:g.74689459C= , CM000664.1:g.74689459C=	GRCh37
NC_000002.10:g.74542967C=	NCBI36
NG_008922.1:g.8079G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1457G=	ENSP00000510501.1:p.Arg486=
ENST00000691308.1:c.829-152G=	ENSP00000509583.1:n.829-152G=
ENST00000448666.7:c.1457G= MANE Select	ENSP00000410992.3:p.Arg486=
ENST00000452063.7:c.1139G=	ENSP00000388201.2:p.Arg380=
ENST00000462443.2:c.632G=	ENSP00000497265.1:p.Arg211=
ENST00000647723.1:c.1400G=
ENST00000647753.1:c.*750G=	ENSP00000497318.1:n.*750G=
ENST00000647771.1:c.*945G=	ENSP00000496788.1:n.*945G=
ENST00000647915.1:c.*750G=	ENSP00000498123.1:n.*750G=
ENST00000648768.1:n.1714G=
ENST00000648810.1:c.632G=	ENSP00000496949.1:p.Arg211=
ENST00000649075.1:c.*385G=	ENSP00000497836.1:n.*385G=
ENST00000649601.1:c.*637G=	ENSP00000496796.1:n.*637G=
ENST00000649777.1:n.1666G=
ENST00000649854.1:c.1090G=
ENST00000650523.1:c.1232G=	ENSP00000497143.1:p.Arg411=
ENST00000233616.8:c.1457G=	ENSP00000233616.4:p.Arg486=
ENST00000409065.5:c.*637G=	ENSP00000386493.1:n.*637G=
ENST00000448666.5:c.1139G=	ENSP00000410992.1:p.Arg380=
ENST00000452063.6:c.1139G=	ENSP00000388201.2:p.Arg380=
ENST00000462189.1:n.1138G=
NM_001146158.1:c.1139G=	NP_001139630.1:p.Arg380=
NM_006302.2:c.1457G=	NP_006293.2:p.Arg486=
NM_006302.3:c.1457G= MANE Select	NP_006293.2:p.Arg486=
NM_001146158.2:c.1139G=	NP_001139630.1:p.Arg380=