Canonical Allele Identifier: CA427033691

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461572G>A , CM000664.2:g.74461572G>A	GRCh38
NC_000002.11:g.74688699G>A , CM000664.1:g.74688699G>A	GRCh37
NC_000002.10:g.74542207G>A	NCBI36
NG_008922.1:g.8839C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006302.3:c.2217C>T MANE Select	NP_006293.2:p.Gly739=
ENST00000448666.7:c.2217C>T MANE Select	ENSP00000410992.3:p.Gly739=
NM_001146158.1:c.1899C>T	NP_001139630.1:p.Gly633=
NM_001146158.2:c.1899C>T	NP_001139630.1:p.Gly633=
NM_006302.2:c.2217C>T	NP_006293.2:p.Gly739=
ENST00000233616.8:c.2217C>T	ENSP00000233616.4:p.Gly739=
ENST00000409065.5:c.*1397C>T	ENSP00000386493.1:n.*1397C>T
ENST00000452063.6:c.1899C>T	ENSP00000388201.2:p.Gly633=
ENST00000452063.7:c.1899C>T	ENSP00000388201.2:p.Gly633=
ENST00000462189.1:n.1898C>T
ENST00000462443.2:c.1392C>T	ENSP00000497265.1:p.Gly464=
ENST00000647723.1:c.2160C>T
ENST00000647753.1:c.*1510C>T	ENSP00000497318.1:n.*1510C>T
ENST00000647771.1:c.*1705C>T	ENSP00000496788.1:n.*1705C>T
ENST00000647915.1:c.*1510C>T	ENSP00000498123.1:n.*1510C>T
ENST00000648768.1:n.2474C>T
ENST00000648810.1:c.1392C>T	ENSP00000496949.1:p.Gly464=
ENST00000649075.1:c.*1145C>T	ENSP00000497836.1:n.*1145C>T
ENST00000649601.1:c.*1397C>T	ENSP00000496796.1:n.*1397C>T
ENST00000649777.1:n.2426C>T
ENST00000649854.1:c.1850C>T
ENST00000690565.1:c.1923C>T	ENSP00000510501.1:p.Gly641=
ENST00000691308.1:c.1143C>T	ENSP00000509583.1:p.Gly381=