Canonical Allele Identifier: CA347366827

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461565T>G , CM000664.2:g.74461565T>G	GRCh38
NC_000002.11:g.74688692T>G , CM000664.1:g.74688692T>G	GRCh37
NC_000002.10:g.74542200T>G	NCBI36
NG_008922.1:g.8846A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006302.3:c.2224A>C MANE Select	NP_006293.2:p.Asn742His
ENST00000448666.7:c.2224A>C MANE Select	ENSP00000410992.3:p.Asn742His
NM_001146158.1:c.1906A>C	NP_001139630.1:p.Asn636His
NM_001146158.2:c.1906A>C	NP_001139630.1:p.Asn636His
NM_006302.2:c.2224A>C	NP_006293.2:p.Asn742His
ENST00000233616.8:c.2224A>C	ENSP00000233616.4:p.Asn742His
ENST00000409065.5:c.*1404A>C	ENSP00000386493.1:n.*1404A>C
ENST00000452063.6:c.1906A>C	ENSP00000388201.2:p.Asn636His
ENST00000452063.7:c.1906A>C	ENSP00000388201.2:p.Asn636His
ENST00000462189.1:n.1905A>C
ENST00000462443.2:c.1399A>C	ENSP00000497265.1:p.Asn467His
ENST00000647723.1:c.2167A>C
ENST00000647753.1:c.*1517A>C	ENSP00000497318.1:n.*1517A>C
ENST00000647771.1:c.*1712A>C	ENSP00000496788.1:n.*1712A>C
ENST00000647915.1:c.*1517A>C	ENSP00000498123.1:n.*1517A>C
ENST00000648768.1:n.2481A>C
ENST00000648810.1:c.1399A>C	ENSP00000496949.1:p.Asn467His
ENST00000649075.1:c.*1152A>C	ENSP00000497836.1:n.*1152A>C
ENST00000649601.1:c.*1404A>C	ENSP00000496796.1:n.*1404A>C
ENST00000649777.1:n.2433A>C
ENST00000649854.1:c.1857A>C
ENST00000690565.1:c.1930A>C	ENSP00000510501.1:p.Asn644His
ENST00000691308.1:c.1150A>C	ENSP00000509583.1:p.Asn384His