Canonical Allele Identifier: CA427034103

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461554A>G , CM000664.2:g.74461554A>G	GRCh38
NC_000002.11:g.74688681A>G , CM000664.1:g.74688681A>G	GRCh37
NC_000002.10:g.74542189A>G	NCBI36
NG_008922.1:g.8857T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1941T>C	ENSP00000510501.1:p.His647=
ENST00000691308.1:c.1161T>C	ENSP00000509583.1:p.His387=
ENST00000448666.7:c.2235T>C MANE Select	ENSP00000410992.3:p.His745=
ENST00000452063.7:c.1917T>C	ENSP00000388201.2:p.His639=
ENST00000462443.2:c.1410T>C	ENSP00000497265.1:p.His470=
ENST00000647723.1:c.2178T>C
ENST00000647753.1:c.*1528T>C	ENSP00000497318.1:n.*1528T>C
ENST00000647771.1:c.*1723T>C	ENSP00000496788.1:n.*1723T>C
ENST00000647915.1:c.*1528T>C	ENSP00000498123.1:n.*1528T>C
ENST00000648768.1:n.2492T>C
ENST00000648810.1:c.1410T>C	ENSP00000496949.1:p.His470=
ENST00000649075.1:c.*1163T>C	ENSP00000497836.1:n.*1163T>C
ENST00000649601.1:c.*1415T>C	ENSP00000496796.1:n.*1415T>C
ENST00000649777.1:n.2444T>C
ENST00000649854.1:c.1868T>C
ENST00000233616.8:c.2235T>C	ENSP00000233616.4:p.His745=
ENST00000409065.5:c.*1415T>C	ENSP00000386493.1:n.*1415T>C
ENST00000452063.6:c.1917T>C	ENSP00000388201.2:p.His639=
ENST00000462189.1:n.1916T>C
NM_001146158.1:c.1917T>C	NP_001139630.1:p.His639=
NM_006302.2:c.2235T>C	NP_006293.2:p.His745=
NM_006302.3:c.2235T>C MANE Select	NP_006293.2:p.His745=
NM_001146158.2:c.1917T>C	NP_001139630.1:p.His639=