Canonical Allele Identifier: CA1261438226

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462233A= , CM000664.2:g.74462233A=	GRCh38
NC_000002.11:g.74689360A= , CM000664.1:g.74689360A=	GRCh37
NC_000002.10:g.74542868A=	NCBI36
NG_008922.1:g.8178T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000690565.1:c.1556T=	ENSP00000510501.1:p.Val519=
ENST00000691308.1:c.829-53T=	ENSP00000509583.1:n.829-53T=
ENST00000448666.7:c.1556T= MANE Select	ENSP00000410992.3:p.Val519=
ENST00000452063.7:c.1238T=	ENSP00000388201.2:p.Val413=
ENST00000462443.2:c.731T=	ENSP00000497265.1:p.Val244=
ENST00000647723.1:c.1499T=
ENST00000647753.1:c.*849T=	ENSP00000497318.1:n.*849T=
ENST00000647771.1:c.*1044T=	ENSP00000496788.1:n.*1044T=
ENST00000647915.1:c.*849T=	ENSP00000498123.1:n.*849T=
ENST00000648768.1:n.1813T=
ENST00000648810.1:c.731T=	ENSP00000496949.1:p.Val244=
ENST00000649075.1:c.*484T=	ENSP00000497836.1:n.*484T=
ENST00000649601.1:c.*736T=	ENSP00000496796.1:n.*736T=
ENST00000649777.1:n.1765T=
ENST00000649854.1:c.1189T=
ENST00000233616.8:c.1556T=	ENSP00000233616.4:p.Val519=
ENST00000409065.5:c.*736T=	ENSP00000386493.1:n.*736T=
ENST00000448666.5:c.1238T=	ENSP00000410992.1:p.Val413=
ENST00000452063.6:c.1238T=	ENSP00000388201.2:p.Val413=
ENST00000462189.1:n.1237T=
NM_001146158.1:c.1238T=	NP_001139630.1:p.Val413=
NM_006302.2:c.1556T=	NP_006293.2:p.Val519=
NM_006302.3:c.1556T= MANE Select	NP_006293.2:p.Val519=
NM_001146158.2:c.1238T=	NP_001139630.1:p.Val413=