Canonical Allele Identifier: CA1724574

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461319C>T , CM000664.2:g.74461319C>T	GRCh38
NC_000002.11:g.74688446C>T , CM000664.1:g.74688446C>T	GRCh37
NC_000002.10:g.74541954C>T	NCBI36
NG_008922.1:g.9092G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.2176G>A	ENSP00000510501.1:p.Gly726Ser
ENST00000691308.1:c.1396G>A	ENSP00000509583.1:p.Gly466Ser
ENST00000448666.7:c.2470G>A MANE Select	ENSP00000410992.3:p.Gly824Ser
ENST00000452063.7:c.2152G>A	ENSP00000388201.2:p.Gly718Ser
ENST00000462443.2:c.1645G>A	ENSP00000497265.1:p.Gly549Ser
ENST00000647723.1:c.2413G>A
ENST00000647753.1:c.*1763G>A	ENSP00000497318.1:n.*1763G>A
ENST00000647771.1:c.*1958G>A	ENSP00000496788.1:n.*1958G>A
ENST00000647915.1:c.*1763G>A	ENSP00000498123.1:n.*1763G>A
ENST00000648768.1:n.2727G>A
ENST00000648810.1:c.1645G>A	ENSP00000496949.1:p.Gly549Ser
ENST00000649075.1:c.*1398G>A	ENSP00000497836.1:n.*1398G>A
ENST00000649601.1:c.*1650G>A	ENSP00000496796.1:n.*1650G>A
ENST00000649777.1:n.2679G>A
ENST00000649854.1:c.2103G>A
ENST00000233616.8:c.2470G>A	ENSP00000233616.4:p.Gly824Ser
ENST00000409065.5:c.*1650G>A	ENSP00000386493.1:n.*1650G>A
ENST00000452063.6:c.2152G>A	ENSP00000388201.2:p.Gly718Ser
ENST00000462189.1:n.2151G>A
NM_001146158.1:c.2152G>A	NP_001139630.1:p.Gly718Ser
NM_006302.2:c.2470G>A	NP_006293.2:p.Gly824Ser
NM_006302.3:c.2470G>A MANE Select	NP_006293.2:p.Gly824Ser
NM_001146158.2:c.2152G>A	NP_001139630.1:p.Gly718Ser