Canonical Allele Identifier: CA1724890

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462907del , CM000664.2:g.74462907del	GRCh38
NC_000002.11:g.74690034del , CM000664.1:g.74690034del	GRCh37
NC_000002.10:g.74543542del	NCBI36
NG_008922.1:g.7504del

Transcript Alleles

HGVS	Amino-acid Change
NM_006302.3:c.882del MANE Select	NP_006293.2:p.Glu295AsnfsTer10
ENST00000448666.7:c.882del MANE Select	ENSP00000410992.3:p.Glu295AsnfsTer10
NM_001146158.1:c.564del	NP_001139630.1:p.Glu189AsnfsTer10
NM_001146158.2:c.564del	NP_001139630.1:p.Glu189AsnfsTer10
NM_006302.2:c.882del	NP_006293.2:p.Glu295AsnfsTer10
ENST00000233616.8:c.882del	ENSP00000233616.4:p.Glu295AsnfsTer10
ENST00000409065.5:c.*62del	ENSP00000386493.1:n.*62del
ENST00000448666.5:c.564del	ENSP00000410992.1:p.Glu189AsnfsTer10
ENST00000452063.6:c.564del	ENSP00000388201.2:p.Glu189AsnfsTer10
ENST00000452063.7:c.564del	ENSP00000388201.2:p.Glu189AsnfsTer10
ENST00000462189.1:n.563del
ENST00000462443.1:n.400del
ENST00000462443.2:c.57del	ENSP00000497265.1:p.Glu20AsnfsTer10
ENST00000489655.1:n.449-73del
ENST00000647723.1:c.825del
ENST00000647753.1:c.*175del	ENSP00000497318.1:n.*175del
ENST00000647771.1:c.*370del	ENSP00000496788.1:n.*370del
ENST00000647915.1:c.*175del	ENSP00000498123.1:n.*175del
ENST00000648768.1:n.1139del
ENST00000648810.1:c.57del	ENSP00000496949.1:p.Glu20AsnfsTer10
ENST00000649075.1:c.828+54del	ENSP00000497836.1:n.828+54del
ENST00000649601.1:c.*62del	ENSP00000496796.1:n.*62del
ENST00000649777.1:n.1091del
ENST00000649854.1:c.515del
ENST00000650523.1:c.657del	ENSP00000497143.1:p.Glu220AsnfsTer10
ENST00000690565.1:c.882del	ENSP00000510501.1:p.Glu295AsnfsTer10
ENST00000691308.1:c.828+54del	ENSP00000509583.1:n.828+54del