Canonical Allele Identifier: CA1261438143

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462026G= , CM000664.2:g.74462026G=	GRCh38
NC_000002.11:g.74689153G= , CM000664.1:g.74689153G=	GRCh37
NC_000002.10:g.74542661G=	NCBI36
NG_008922.1:g.8385C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1763C=	ENSP00000510501.1:p.Ala588=
ENST00000691308.1:c.983C=	ENSP00000509583.1:p.Ala328=
ENST00000448666.7:c.1763C= MANE Select	ENSP00000410992.3:p.Ala588=
ENST00000452063.7:c.1445C=	ENSP00000388201.2:p.Ala482=
ENST00000462443.2:c.938C=	ENSP00000497265.1:p.Ala313=
ENST00000647723.1:c.1706C=
ENST00000647753.1:c.*1056C=	ENSP00000497318.1:n.*1056C=
ENST00000647771.1:c.*1251C=	ENSP00000496788.1:n.*1251C=
ENST00000647915.1:c.*1056C=	ENSP00000498123.1:n.*1056C=
ENST00000648768.1:n.2020C=
ENST00000648810.1:c.938C=	ENSP00000496949.1:p.Ala313=
ENST00000649075.1:c.*691C=	ENSP00000497836.1:n.*691C=
ENST00000649601.1:c.*943C=	ENSP00000496796.1:n.*943C=
ENST00000649777.1:n.1972C=
ENST00000649854.1:c.1396C=
ENST00000233616.8:c.1763C=	ENSP00000233616.4:p.Ala588=
ENST00000409065.5:c.*943C=	ENSP00000386493.1:n.*943C=
ENST00000448666.5:c.1445C=	ENSP00000410992.1:p.Ala482=
ENST00000452063.6:c.1445C=	ENSP00000388201.2:p.Ala482=
ENST00000462189.1:n.1444C=
NM_001146158.1:c.1445C=	NP_001139630.1:p.Ala482=
NM_006302.2:c.1763C=	NP_006293.2:p.Ala588=
NM_006302.3:c.1763C= MANE Select	NP_006293.2:p.Ala588=
NM_001146158.2:c.1445C=	NP_001139630.1:p.Ala482=