Canonical Allele Identifier: CA427033699

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461578A>G , CM000664.2:g.74461578A>G	GRCh38
NC_000002.11:g.74688705A>G , CM000664.1:g.74688705A>G	GRCh37
NC_000002.10:g.74542213A>G	NCBI36
NG_008922.1:g.8833T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006302.3:c.2211T>C MANE Select	NP_006293.2:p.Phe737=
ENST00000448666.7:c.2211T>C MANE Select	ENSP00000410992.3:p.Phe737=
NM_001146158.1:c.1893T>C	NP_001139630.1:p.Phe631=
NM_001146158.2:c.1893T>C	NP_001139630.1:p.Phe631=
NM_006302.2:c.2211T>C	NP_006293.2:p.Phe737=
ENST00000233616.8:c.2211T>C	ENSP00000233616.4:p.Phe737=
ENST00000409065.5:c.*1391T>C	ENSP00000386493.1:n.*1391T>C
ENST00000452063.6:c.1893T>C	ENSP00000388201.2:p.Phe631=
ENST00000452063.7:c.1893T>C	ENSP00000388201.2:p.Phe631=
ENST00000462189.1:n.1892T>C
ENST00000462443.2:c.1386T>C	ENSP00000497265.1:p.Phe462=
ENST00000647723.1:c.2154T>C
ENST00000647753.1:c.*1504T>C	ENSP00000497318.1:n.*1504T>C
ENST00000647771.1:c.*1699T>C	ENSP00000496788.1:n.*1699T>C
ENST00000647915.1:c.*1504T>C	ENSP00000498123.1:n.*1504T>C
ENST00000648768.1:n.2468T>C
ENST00000648810.1:c.1386T>C	ENSP00000496949.1:p.Phe462=
ENST00000649075.1:c.*1139T>C	ENSP00000497836.1:n.*1139T>C
ENST00000649601.1:c.*1391T>C	ENSP00000496796.1:n.*1391T>C
ENST00000649777.1:n.2420T>C
ENST00000649854.1:c.1844T>C
ENST00000690565.1:c.1917T>C	ENSP00000510501.1:p.Phe639=
ENST00000691308.1:c.1137T>C	ENSP00000509583.1:p.Phe379=