Canonical Allele Identifier: CA1724678

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461768C>G , CM000664.2:g.74461768C>G	GRCh38
NC_000002.11:g.74688895C>G , CM000664.1:g.74688895C>G	GRCh37
NC_000002.10:g.74542403C>G	NCBI36
NG_008922.1:g.8643G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006302.3:c.2021G>C MANE Select	NP_006293.2:p.Arg674Pro
ENST00000448666.7:c.2021G>C MANE Select	ENSP00000410992.3:p.Arg674Pro
NM_001146158.1:c.1703G>C	NP_001139630.1:p.Arg568Pro
NM_001146158.2:c.1703G>C	NP_001139630.1:p.Arg568Pro
NM_006302.2:c.2021G>C	NP_006293.2:p.Arg674Pro
ENST00000233616.8:c.2021G>C	ENSP00000233616.4:p.Arg674Pro
ENST00000409065.5:c.*1201G>C	ENSP00000386493.1:n.*1201G>C
ENST00000452063.6:c.1703G>C	ENSP00000388201.2:p.Arg568Pro
ENST00000452063.7:c.1703G>C	ENSP00000388201.2:p.Arg568Pro
ENST00000462189.1:n.1702G>C
ENST00000462443.2:c.1196G>C	ENSP00000497265.1:p.Arg399Pro
ENST00000647723.1:c.1964G>C
ENST00000647753.1:c.*1314G>C	ENSP00000497318.1:n.*1314G>C
ENST00000647771.1:c.*1509G>C	ENSP00000496788.1:n.*1509G>C
ENST00000647915.1:c.*1314G>C	ENSP00000498123.1:n.*1314G>C
ENST00000648768.1:n.2278G>C
ENST00000648810.1:c.1196G>C	ENSP00000496949.1:p.Arg399Pro
ENST00000649075.1:c.*949G>C	ENSP00000497836.1:n.*949G>C
ENST00000649601.1:c.*1201G>C	ENSP00000496796.1:n.*1201G>C
ENST00000649777.1:n.2230G>C
ENST00000649854.1:c.1654G>C
ENST00000690565.1:c.1856-129G>C	ENSP00000510501.1:n.1856-129G>C
ENST00000691308.1:c.1076-129G>C	ENSP00000509583.1:n.1076-129G>C