Canonical Allele Identifier: CA427034182

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461776C>A , CM000664.2:g.74461776C>A	GRCh38
NC_000002.11:g.74688903C>A , CM000664.1:g.74688903C>A	GRCh37
NC_000002.10:g.74542411C>A	NCBI36
NG_008922.1:g.8635G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1856-137G>T	ENSP00000510501.1:n.1856-137G>T
ENST00000691308.1:c.1076-137G>T	ENSP00000509583.1:n.1076-137G>T
ENST00000448666.7:c.2013G>T MANE Select	ENSP00000410992.3:p.Gly671=
ENST00000452063.7:c.1695G>T	ENSP00000388201.2:p.Gly565=
ENST00000462443.2:c.1188G>T	ENSP00000497265.1:p.Gly396=
ENST00000647723.1:c.1956G>T
ENST00000647753.1:c.*1306G>T	ENSP00000497318.1:n.*1306G>T
ENST00000647771.1:c.*1501G>T	ENSP00000496788.1:n.*1501G>T
ENST00000647915.1:c.*1306G>T	ENSP00000498123.1:n.*1306G>T
ENST00000648768.1:n.2270G>T
ENST00000648810.1:c.1188G>T	ENSP00000496949.1:p.Gly396=
ENST00000649075.1:c.*941G>T	ENSP00000497836.1:n.*941G>T
ENST00000649601.1:c.*1193G>T	ENSP00000496796.1:n.*1193G>T
ENST00000649777.1:n.2222G>T
ENST00000649854.1:c.1646G>T
ENST00000233616.8:c.2013G>T	ENSP00000233616.4:p.Gly671=
ENST00000409065.5:c.*1193G>T	ENSP00000386493.1:n.*1193G>T
ENST00000452063.6:c.1695G>T	ENSP00000388201.2:p.Gly565=
ENST00000462189.1:n.1694G>T
NM_001146158.1:c.1695G>T	NP_001139630.1:p.Gly565=
NM_006302.2:c.2013G>T	NP_006293.2:p.Gly671=
NM_006302.3:c.2013G>T MANE Select	NP_006293.2:p.Gly671=
NM_001146158.2:c.1695G>T	NP_001139630.1:p.Gly565=