Canonical Allele Identifier: CA1724567

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461284T>G , CM000664.2:g.74461284T>G	GRCh38
NC_000002.11:g.74688411T>G , CM000664.1:g.74688411T>G	GRCh37
NC_000002.10:g.74541919T>G	NCBI36
NG_008922.1:g.9127A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.2211A>C	ENSP00000510501.1:p.Glu737Asp
ENST00000691308.1:c.1431A>C	ENSP00000509583.1:p.Glu477Asp
ENST00000448666.7:c.2505A>C MANE Select	ENSP00000410992.3:p.Glu835Asp
ENST00000452063.7:c.2187A>C	ENSP00000388201.2:p.Glu729Asp
ENST00000462443.2:c.1680A>C	ENSP00000497265.1:p.Glu560Asp
ENST00000647723.1:c.2448A>C
ENST00000647753.1:c.*1798A>C	ENSP00000497318.1:n.*1798A>C
ENST00000647771.1:c.*1993A>C	ENSP00000496788.1:n.*1993A>C
ENST00000647915.1:c.*1798A>C	ENSP00000498123.1:n.*1798A>C
ENST00000648768.1:n.2762A>C
ENST00000648810.1:c.1680A>C	ENSP00000496949.1:p.Glu560Asp
ENST00000649075.1:c.*1433A>C	ENSP00000497836.1:n.*1433A>C
ENST00000649601.1:c.*1685A>C	ENSP00000496796.1:n.*1685A>C
ENST00000649777.1:n.2714A>C
ENST00000649854.1:c.2138A>C
ENST00000233616.8:c.2505A>C	ENSP00000233616.4:p.Glu835Asp
ENST00000409065.5:c.*1685A>C	ENSP00000386493.1:n.*1685A>C
ENST00000452063.6:c.2187A>C	ENSP00000388201.2:p.Glu729Asp
ENST00000462189.1:n.2186A>C
NM_001146158.1:c.2187A>C	NP_001139630.1:p.Glu729Asp
NM_006302.2:c.2505A>C	NP_006293.2:p.Glu835Asp
NM_006302.3:c.2505A>C MANE Select	NP_006293.2:p.Glu835Asp
NM_001146158.2:c.2187A>C	NP_001139630.1:p.Glu729Asp