Canonical Allele Identifier: CA1724887

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462895G>A , CM000664.2:g.74462895G>A	GRCh38
NC_000002.11:g.74690022G>A , CM000664.1:g.74690022G>A	GRCh37
NC_000002.10:g.74543530G>A	NCBI36
NG_008922.1:g.7516C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006302.3:c.894C>T MANE Select	NP_006293.2:p.Leu298=
ENST00000448666.7:c.894C>T MANE Select	ENSP00000410992.3:p.Leu298=
NM_001146158.1:c.576C>T	NP_001139630.1:p.Leu192=
NM_001146158.2:c.576C>T	NP_001139630.1:p.Leu192=
NM_006302.2:c.894C>T	NP_006293.2:p.Leu298=
ENST00000233616.8:c.894C>T	ENSP00000233616.4:p.Leu298=
ENST00000409065.5:c.*74C>T	ENSP00000386493.1:n.*74C>T
ENST00000448666.5:c.576C>T	ENSP00000410992.1:p.Leu192=
ENST00000452063.6:c.576C>T	ENSP00000388201.2:p.Leu192=
ENST00000452063.7:c.576C>T	ENSP00000388201.2:p.Leu192=
ENST00000462189.1:n.575C>T
ENST00000462443.1:n.412C>T
ENST00000462443.2:c.69C>T	ENSP00000497265.1:p.Leu23=
ENST00000489655.1:n.449-61C>T
ENST00000647723.1:c.837C>T
ENST00000647753.1:c.*187C>T	ENSP00000497318.1:n.*187C>T
ENST00000647771.1:c.*382C>T	ENSP00000496788.1:n.*382C>T
ENST00000647915.1:c.*187C>T	ENSP00000498123.1:n.*187C>T
ENST00000648768.1:n.1151C>T
ENST00000648810.1:c.69C>T	ENSP00000496949.1:p.Leu23=
ENST00000649075.1:c.828+66C>T	ENSP00000497836.1:n.828+66C>T
ENST00000649601.1:c.*74C>T	ENSP00000496796.1:n.*74C>T
ENST00000649777.1:n.1103C>T
ENST00000649854.1:c.527C>T
ENST00000650523.1:c.669C>T	ENSP00000497143.1:p.Leu223=
ENST00000690565.1:c.894C>T	ENSP00000510501.1:p.Leu298=
ENST00000691308.1:c.828+66C>T	ENSP00000509583.1:n.828+66C>T