Canonical Allele Identifier: CA916568188

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461801dup , CM000664.2:g.74461801dup	GRCh38
NC_000002.11:g.74688928dup , CM000664.1:g.74688928dup	GRCh37
NC_000002.10:g.74542436dup	NCBI36
NG_008922.1:g.8610dup

Transcript Alleles

HGVS	Amino-acid Change
NM_006302.3:c.1988dup MANE Select	NP_006293.2:p.Leu664AlafsTer?
ENST00000448666.7:c.1988dup MANE Select	ENSP00000410992.3:p.Leu664AlafsTer?
NM_001146158.1:c.1670dup	NP_001139630.1:p.Leu558AlafsTer?
NM_001146158.2:c.1670dup	NP_001139630.1:p.Leu558AlafsTer?
NM_006302.2:c.1988dup	NP_006293.2:p.Leu664AlafsTer?
ENST00000233616.8:c.1988dup	ENSP00000233616.4:p.Leu664AlafsTer?
ENST00000409065.5:c.*1168dup	ENSP00000386493.1:n.*1168dup
ENST00000452063.6:c.1670dup	ENSP00000388201.2:p.Leu558AlafsTer?
ENST00000452063.7:c.1670dup	ENSP00000388201.2:p.Leu558AlafsTer?
ENST00000462189.1:n.1669dup
ENST00000462443.2:c.1163dup	ENSP00000497265.1:p.Leu389AlafsTer?
ENST00000647723.1:c.1931dup
ENST00000647753.1:c.*1281dup	ENSP00000497318.1:n.*1281dup
ENST00000647771.1:c.*1476dup	ENSP00000496788.1:n.*1476dup
ENST00000647915.1:c.*1281dup	ENSP00000498123.1:n.*1281dup
ENST00000648768.1:n.2245dup
ENST00000648810.1:c.1163dup	ENSP00000496949.1:p.Leu389AlafsTer?
ENST00000649075.1:c.*916dup	ENSP00000497836.1:n.*916dup
ENST00000649601.1:c.*1168dup	ENSP00000496796.1:n.*1168dup
ENST00000649777.1:n.2197dup
ENST00000649854.1:c.1621dup
ENST00000690565.1:c.1855+133dup	ENSP00000510501.1:n.1855+133dup
ENST00000691308.1:c.1075+133dup	ENSP00000509583.1:n.1075+133dup