Canonical Allele Identifier: CA427033802

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74461443T>C , CM000664.2:g.74461443T>C	GRCh38
NC_000002.11:g.74688570T>C , CM000664.1:g.74688570T>C	GRCh37
NC_000002.10:g.74542078T>C	NCBI36
NG_008922.1:g.8968A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.2052A>G	ENSP00000510501.1:p.Lys684=
ENST00000691308.1:c.1272A>G	ENSP00000509583.1:p.Lys424=
ENST00000448666.7:c.2346A>G MANE Select	ENSP00000410992.3:p.Lys782=
ENST00000452063.7:c.2028A>G	ENSP00000388201.2:p.Lys676=
ENST00000462443.2:c.1521A>G	ENSP00000497265.1:p.Lys507=
ENST00000647723.1:c.2289A>G
ENST00000647753.1:c.*1639A>G	ENSP00000497318.1:n.*1639A>G
ENST00000647771.1:c.*1834A>G	ENSP00000496788.1:n.*1834A>G
ENST00000647915.1:c.*1639A>G	ENSP00000498123.1:n.*1639A>G
ENST00000648768.1:n.2603A>G
ENST00000648810.1:c.1521A>G	ENSP00000496949.1:p.Lys507=
ENST00000649075.1:c.*1274A>G	ENSP00000497836.1:n.*1274A>G
ENST00000649601.1:c.*1526A>G	ENSP00000496796.1:n.*1526A>G
ENST00000649777.1:n.2555A>G
ENST00000649854.1:c.1979A>G
ENST00000233616.8:c.2346A>G	ENSP00000233616.4:p.Lys782=
ENST00000409065.5:c.*1526A>G	ENSP00000386493.1:n.*1526A>G
ENST00000452063.6:c.2028A>G	ENSP00000388201.2:p.Lys676=
ENST00000462189.1:n.2027A>G
NM_001146158.1:c.2028A>G	NP_001139630.1:p.Lys676=
NM_006302.2:c.2346A>G	NP_006293.2:p.Lys782=
NM_006302.3:c.2346A>G MANE Select	NP_006293.2:p.Lys782=
NM_001146158.2:c.2028A>G	NP_001139630.1:p.Lys676=