Canonical Allele Identifier: CA1724596

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461419G>A , CM000664.2:g.74461419G>A	GRCh38
NC_000002.11:g.74688546G>A , CM000664.1:g.74688546G>A	GRCh37
NC_000002.10:g.74542054G>A	NCBI36
NG_008922.1:g.8992C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006302.3:c.2370C>T MANE Select	NP_006293.2:p.Asn790=
ENST00000448666.7:c.2370C>T MANE Select	ENSP00000410992.3:p.Asn790=
NM_001146158.1:c.2052C>T	NP_001139630.1:p.Asn684=
NM_001146158.2:c.2052C>T	NP_001139630.1:p.Asn684=
NM_006302.2:c.2370C>T	NP_006293.2:p.Asn790=
ENST00000233616.8:c.2370C>T	ENSP00000233616.4:p.Asn790=
ENST00000409065.5:c.*1550C>T	ENSP00000386493.1:n.*1550C>T
ENST00000452063.6:c.2052C>T	ENSP00000388201.2:p.Asn684=
ENST00000452063.7:c.2052C>T	ENSP00000388201.2:p.Asn684=
ENST00000462189.1:n.2051C>T
ENST00000462443.2:c.1545C>T	ENSP00000497265.1:p.Asn515=
ENST00000647723.1:c.2313C>T
ENST00000647753.1:c.*1663C>T	ENSP00000497318.1:n.*1663C>T
ENST00000647771.1:c.*1858C>T	ENSP00000496788.1:n.*1858C>T
ENST00000647915.1:c.*1663C>T	ENSP00000498123.1:n.*1663C>T
ENST00000648768.1:n.2627C>T
ENST00000648810.1:c.1545C>T	ENSP00000496949.1:p.Asn515=
ENST00000649075.1:c.*1298C>T	ENSP00000497836.1:n.*1298C>T
ENST00000649601.1:c.*1550C>T	ENSP00000496796.1:n.*1550C>T
ENST00000649777.1:n.2579C>T
ENST00000649854.1:c.2003C>T
ENST00000690565.1:c.2076C>T	ENSP00000510501.1:p.Asn692=
ENST00000691308.1:c.1296C>T	ENSP00000509583.1:p.Asn432=