Canonical Allele Identifier: CA1724592

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461414A>G , CM000664.2:g.74461414A>G	GRCh38
NC_000002.11:g.74688541A>G , CM000664.1:g.74688541A>G	GRCh37
NC_000002.10:g.74542049A>G	NCBI36
NG_008922.1:g.8997T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.2081T>C	ENSP00000510501.1:p.Val694Ala
ENST00000691308.1:c.1301T>C	ENSP00000509583.1:p.Val434Ala
ENST00000448666.7:c.2375T>C MANE Select	ENSP00000410992.3:p.Val792Ala
ENST00000452063.7:c.2057T>C	ENSP00000388201.2:p.Val686Ala
ENST00000462443.2:c.1550T>C	ENSP00000497265.1:p.Val517Ala
ENST00000647723.1:c.2318T>C
ENST00000647753.1:c.*1668T>C	ENSP00000497318.1:n.*1668T>C
ENST00000647771.1:c.*1863T>C	ENSP00000496788.1:n.*1863T>C
ENST00000647915.1:c.*1668T>C	ENSP00000498123.1:n.*1668T>C
ENST00000648768.1:n.2632T>C
ENST00000648810.1:c.1550T>C	ENSP00000496949.1:p.Val517Ala
ENST00000649075.1:c.*1303T>C	ENSP00000497836.1:n.*1303T>C
ENST00000649601.1:c.*1555T>C	ENSP00000496796.1:n.*1555T>C
ENST00000649777.1:n.2584T>C
ENST00000649854.1:c.2008T>C
ENST00000233616.8:c.2375T>C	ENSP00000233616.4:p.Val792Ala
ENST00000409065.5:c.*1555T>C	ENSP00000386493.1:n.*1555T>C
ENST00000452063.6:c.2057T>C	ENSP00000388201.2:p.Val686Ala
ENST00000462189.1:n.2056T>C
NM_001146158.1:c.2057T>C	NP_001139630.1:p.Val686Ala
NM_006302.2:c.2375T>C	NP_006293.2:p.Val792Ala
NM_006302.3:c.2375T>C MANE Select	NP_006293.2:p.Val792Ala
NM_001146158.2:c.2057T>C	NP_001139630.1:p.Val686Ala