Canonical Allele Identifier: CA1724588

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461391G>A , CM000664.2:g.74461391G>A	GRCh38
NC_000002.11:g.74688518G>A , CM000664.1:g.74688518G>A	GRCh37
NC_000002.10:g.74542026G>A	NCBI36
NG_008922.1:g.9020C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.2104C>T	ENSP00000510501.1:p.Gln702Ter
ENST00000691308.1:c.1324C>T	ENSP00000509583.1:p.Gln442Ter
ENST00000448666.7:c.2398C>T MANE Select	ENSP00000410992.3:p.Gln800Ter
ENST00000452063.7:c.2080C>T	ENSP00000388201.2:p.Gln694Ter
ENST00000462443.2:c.1573C>T	ENSP00000497265.1:p.Gln525Ter
ENST00000647723.1:c.2341C>T
ENST00000647753.1:c.*1691C>T	ENSP00000497318.1:n.*1691C>T
ENST00000647771.1:c.*1886C>T	ENSP00000496788.1:n.*1886C>T
ENST00000647915.1:c.*1691C>T	ENSP00000498123.1:n.*1691C>T
ENST00000648768.1:n.2655C>T
ENST00000648810.1:c.1573C>T	ENSP00000496949.1:p.Gln525Ter
ENST00000649075.1:c.*1326C>T	ENSP00000497836.1:n.*1326C>T
ENST00000649601.1:c.*1578C>T	ENSP00000496796.1:n.*1578C>T
ENST00000649777.1:n.2607C>T
ENST00000649854.1:c.2031C>T
ENST00000233616.8:c.2398C>T	ENSP00000233616.4:p.Gln800Ter
ENST00000409065.5:c.*1578C>T	ENSP00000386493.1:n.*1578C>T
ENST00000452063.6:c.2080C>T	ENSP00000388201.2:p.Gln694Ter
ENST00000462189.1:n.2079C>T
NM_001146158.1:c.2080C>T	NP_001139630.1:p.Gln694Ter
NM_006302.2:c.2398C>T	NP_006293.2:p.Gln800Ter
NM_006302.3:c.2398C>T MANE Select	NP_006293.2:p.Gln800Ter
NM_001146158.2:c.2080C>T	NP_001139630.1:p.Gln694Ter