Canonical Allele Identifier: CA148473

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74465064C>T , CM000664.2:g.74465064C>T	GRCh38
NC_000002.11:g.74692191C>T , CM000664.1:g.74692191C>T	GRCh37
NC_000002.10:g.74545699C>T	NCBI36
NG_008922.1:g.5347G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.184G>A	ENSP00000510501.1:p.Val62Met
ENST00000691308.1:c.184G>A	ENSP00000509583.1:p.Val62Met
ENST00000448666.7:c.184G>A MANE Select	ENSP00000410992.3:p.Val62Met
ENST00000452063.7:c.-58-77G>A	ENSP00000388201.2:n.-58-77G>A
ENST00000462443.2:c.-247+250G>A	ENSP00000497265.1:n.-247+250G>A
ENST00000647723.1:c.182G>A
ENST00000647753.1:c.184G>A	ENSP00000497318.1:p.Val62Met
ENST00000647771.1:c.166+18G>A	ENSP00000496788.1:n.166+18G>A
ENST00000647915.1:c.-58-77G>A	ENSP00000498123.1:n.-58-77G>A
ENST00000648768.1:n.264G>A
ENST00000648810.1:c.-192+250G>A	ENSP00000496949.1:n.-192+250G>A
ENST00000649075.1:c.184G>A	ENSP00000497836.1:p.Val62Met
ENST00000649601.1:c.-58-77G>A	ENSP00000496796.1:n.-58-77G>A
ENST00000649777.1:n.220G>A
ENST00000649854.1:c.99G>A
ENST00000650523.1:c.184G>A	ENSP00000497143.1:p.Val62Met
ENST00000233616.8:c.184G>A	ENSP00000233616.4:p.Val62Met
ENST00000409065.5:c.184G>A	ENSP00000386493.1:p.Val62Met
ENST00000414701.1:c.-6+250G>A	ENSP00000396298.1:n.-6+250G>A
ENST00000448666.5:c.-58-77G>A	ENSP00000410992.1:n.-58-77G>A
ENST00000452063.6:c.-58-77G>A	ENSP00000388201.2:n.-58-77G>A
ENST00000462443.1:n.97+250G>A
ENST00000486036.1:n.337G>A
NM_001146158.1:c.-58-77G>A	NP_001139630.1:n.-58-77G>A
NM_006302.2:c.184G>A	NP_006293.2:p.Val62Met
NM_006302.3:c.184G>A MANE Select	NP_006293.2:p.Val62Met
NM_001146158.2:c.-58-77G>A	NP_001139630.1:n.-58-77G>A