Canonical Allele Identifier: CA427033574

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461346G>T , CM000664.2:g.74461346G>T	GRCh38
NC_000002.11:g.74688473G>T , CM000664.1:g.74688473G>T	GRCh37
NC_000002.10:g.74541981G>T	NCBI36
NG_008922.1:g.9065C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.2149C>A	ENSP00000510501.1:p.Arg717=
ENST00000691308.1:c.1369C>A	ENSP00000509583.1:p.Arg457=
ENST00000448666.7:c.2443C>A MANE Select	ENSP00000410992.3:p.Arg815=
ENST00000452063.7:c.2125C>A	ENSP00000388201.2:p.Arg709=
ENST00000462443.2:c.1618C>A	ENSP00000497265.1:p.Arg540=
ENST00000647723.1:c.2386C>A
ENST00000647753.1:c.*1736C>A	ENSP00000497318.1:n.*1736C>A
ENST00000647771.1:c.*1931C>A	ENSP00000496788.1:n.*1931C>A
ENST00000647915.1:c.*1736C>A	ENSP00000498123.1:n.*1736C>A
ENST00000648768.1:n.2700C>A
ENST00000648810.1:c.1618C>A	ENSP00000496949.1:p.Arg540=
ENST00000649075.1:c.*1371C>A	ENSP00000497836.1:n.*1371C>A
ENST00000649601.1:c.*1623C>A	ENSP00000496796.1:n.*1623C>A
ENST00000649777.1:n.2652C>A
ENST00000649854.1:c.2076C>A
ENST00000233616.8:c.2443C>A	ENSP00000233616.4:p.Arg815=
ENST00000409065.5:c.*1623C>A	ENSP00000386493.1:n.*1623C>A
ENST00000452063.6:c.2125C>A	ENSP00000388201.2:p.Arg709=
ENST00000462189.1:n.2124C>A
NM_001146158.1:c.2125C>A	NP_001139630.1:p.Arg709=
NM_006302.2:c.2443C>A	NP_006293.2:p.Arg815=
NM_006302.3:c.2443C>A MANE Select	NP_006293.2:p.Arg815=
NM_001146158.2:c.2125C>A	NP_001139630.1:p.Arg709=