Canonical Allele Identifier: CA1261438274

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462346A= , CM000664.2:g.74462346A=	GRCh38
NC_000002.11:g.74689473A= , CM000664.1:g.74689473A=	GRCh37
NC_000002.10:g.74542981A=	NCBI36
NG_008922.1:g.8065T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000690565.1:c.1443T=	ENSP00000510501.1:p.Asp481=
ENST00000691308.1:c.829-166T=	ENSP00000509583.1:n.829-166T=
ENST00000448666.7:c.1443T= MANE Select	ENSP00000410992.3:p.Asp481=
ENST00000452063.7:c.1125T=	ENSP00000388201.2:p.Asp375=
ENST00000462443.2:c.618T=	ENSP00000497265.1:p.Asp206=
ENST00000647723.1:c.1386T=
ENST00000647753.1:c.*736T=	ENSP00000497318.1:n.*736T=
ENST00000647771.1:c.*931T=	ENSP00000496788.1:n.*931T=
ENST00000647915.1:c.*736T=	ENSP00000498123.1:n.*736T=
ENST00000648768.1:n.1700T=
ENST00000648810.1:c.618T=	ENSP00000496949.1:p.Asp206=
ENST00000649075.1:c.*371T=	ENSP00000497836.1:n.*371T=
ENST00000649601.1:c.*623T=	ENSP00000496796.1:n.*623T=
ENST00000649777.1:n.1652T=
ENST00000649854.1:c.1076T=
ENST00000650523.1:c.1218T=	ENSP00000497143.1:p.Asp406=
ENST00000233616.8:c.1443T=	ENSP00000233616.4:p.Asp481=
ENST00000409065.5:c.*623T=	ENSP00000386493.1:n.*623T=
ENST00000448666.5:c.1125T=	ENSP00000410992.1:p.Asp375=
ENST00000452063.6:c.1125T=	ENSP00000388201.2:p.Asp375=
ENST00000462189.1:n.1124T=
NM_001146158.1:c.1125T=	NP_001139630.1:p.Asp375=
NM_006302.2:c.1443T=	NP_006293.2:p.Asp481=
NM_006302.3:c.1443T= MANE Select	NP_006293.2:p.Asp481=
NM_001146158.2:c.1125T=	NP_001139630.1:p.Asp375=