Canonical Allele Identifier: CA1261438228

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462238C= , CM000664.2:g.74462238C=	GRCh38
NC_000002.11:g.74689365C= , CM000664.1:g.74689365C=	GRCh37
NC_000002.10:g.74542873C=	NCBI36
NG_008922.1:g.8173G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000690565.1:c.1551G=	ENSP00000510501.1:p.Leu517=
ENST00000691308.1:c.829-58G=	ENSP00000509583.1:n.829-58G=
ENST00000448666.7:c.1551G= MANE Select	ENSP00000410992.3:p.Leu517=
ENST00000452063.7:c.1233G=	ENSP00000388201.2:p.Leu411=
ENST00000462443.2:c.726G=	ENSP00000497265.1:p.Leu242=
ENST00000647723.1:c.1494G=
ENST00000647753.1:c.*844G=	ENSP00000497318.1:n.*844G=
ENST00000647771.1:c.*1039G=	ENSP00000496788.1:n.*1039G=
ENST00000647915.1:c.*844G=	ENSP00000498123.1:n.*844G=
ENST00000648768.1:n.1808G=
ENST00000648810.1:c.726G=	ENSP00000496949.1:p.Leu242=
ENST00000649075.1:c.*479G=	ENSP00000497836.1:n.*479G=
ENST00000649601.1:c.*731G=	ENSP00000496796.1:n.*731G=
ENST00000649777.1:n.1760G=
ENST00000649854.1:c.1184G=
ENST00000233616.8:c.1551G=	ENSP00000233616.4:p.Leu517=
ENST00000409065.5:c.*731G=	ENSP00000386493.1:n.*731G=
ENST00000448666.5:c.1233G=	ENSP00000410992.1:p.Leu411=
ENST00000452063.6:c.1233G=	ENSP00000388201.2:p.Leu411=
ENST00000462189.1:n.1232G=
NM_001146158.1:c.1233G=	NP_001139630.1:p.Leu411=
NM_006302.2:c.1551G=	NP_006293.2:p.Leu517=
NM_006302.3:c.1551G= MANE Select	NP_006293.2:p.Leu517=
NM_001146158.2:c.1233G=	NP_001139630.1:p.Leu411=