Canonical Allele Identifier: CA1724603

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461437G>A , CM000664.2:g.74461437G>A	GRCh38
NC_000002.11:g.74688564G>A , CM000664.1:g.74688564G>A	GRCh37
NC_000002.10:g.74542072G>A	NCBI36
NG_008922.1:g.8974C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.2058C>T	ENSP00000510501.1:p.His686=
ENST00000691308.1:c.1278C>T	ENSP00000509583.1:p.His426=
ENST00000448666.7:c.2352C>T MANE Select	ENSP00000410992.3:p.His784=
ENST00000452063.7:c.2034C>T	ENSP00000388201.2:p.His678=
ENST00000462443.2:c.1527C>T	ENSP00000497265.1:p.His509=
ENST00000647723.1:c.2295C>T
ENST00000647753.1:c.*1645C>T	ENSP00000497318.1:n.*1645C>T
ENST00000647771.1:c.*1840C>T	ENSP00000496788.1:n.*1840C>T
ENST00000647915.1:c.*1645C>T	ENSP00000498123.1:n.*1645C>T
ENST00000648768.1:n.2609C>T
ENST00000648810.1:c.1527C>T	ENSP00000496949.1:p.His509=
ENST00000649075.1:c.*1280C>T	ENSP00000497836.1:n.*1280C>T
ENST00000649601.1:c.*1532C>T	ENSP00000496796.1:n.*1532C>T
ENST00000649777.1:n.2561C>T
ENST00000649854.1:c.1985C>T
ENST00000233616.8:c.2352C>T	ENSP00000233616.4:p.His784=
ENST00000409065.5:c.*1532C>T	ENSP00000386493.1:n.*1532C>T
ENST00000452063.6:c.2034C>T	ENSP00000388201.2:p.His678=
ENST00000462189.1:n.2033C>T
NM_001146158.1:c.2034C>T	NP_001139630.1:p.His678=
NM_006302.2:c.2352C>T	NP_006293.2:p.His784=
NM_006302.3:c.2352C>T MANE Select	NP_006293.2:p.His784=
NM_001146158.2:c.2034C>T	NP_001139630.1:p.His678=