Canonical Allele Identifier: CA427034633

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689155C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462028C>T , CM000664.2:g.74462028C>T	GRCh38
NC_000002.11:g.74689155C>T , CM000664.1:g.74689155C>T	GRCh37
NC_000002.10:g.74542663C>T	NCBI36
NG_008922.1:g.8383G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1761G>A	ENSP00000510501.1:p.Arg587=
ENST00000691308.1:c.981G>A	ENSP00000509583.1:p.Arg327=
ENST00000448666.7:c.1761G>A MANE Select	ENSP00000410992.3:p.Arg587=
ENST00000452063.7:c.1443G>A	ENSP00000388201.2:p.Arg481=
ENST00000462443.2:c.936G>A	ENSP00000497265.1:p.Arg312=
ENST00000647723.1:c.1704G>A
ENST00000647753.1:c.*1054G>A	ENSP00000497318.1:n.*1054G>A
ENST00000647771.1:c.*1249G>A	ENSP00000496788.1:n.*1249G>A
ENST00000647915.1:c.*1054G>A	ENSP00000498123.1:n.*1054G>A
ENST00000648768.1:n.2018G>A
ENST00000648810.1:c.936G>A	ENSP00000496949.1:p.Arg312=
ENST00000649075.1:c.*689G>A	ENSP00000497836.1:n.*689G>A
ENST00000649601.1:c.*941G>A	ENSP00000496796.1:n.*941G>A
ENST00000649777.1:n.1970G>A
ENST00000649854.1:c.1394G>A
ENST00000233616.8:c.1761G>A	ENSP00000233616.4:p.Arg587=
ENST00000409065.5:c.*941G>A	ENSP00000386493.1:n.*941G>A
ENST00000448666.5:c.1443G>A	ENSP00000410992.1:p.Arg481=
ENST00000452063.6:c.1443G>A	ENSP00000388201.2:p.Arg481=
ENST00000462189.1:n.1442G>A
NM_001146158.1:c.1443G>A	NP_001139630.1:p.Arg481=
NM_006302.2:c.1761G>A	NP_006293.2:p.Arg587=
NM_006302.3:c.1761G>A MANE Select	NP_006293.2:p.Arg587=
NM_001146158.2:c.1443G>A	NP_001139630.1:p.Arg481=