Canonical Allele Identifier: CA427034389

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689460T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462333T>G , CM000664.2:g.74462333T>G	GRCh38
NC_000002.11:g.74689460T>G , CM000664.1:g.74689460T>G	GRCh37
NC_000002.10:g.74542968T>G	NCBI36
NG_008922.1:g.8078A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1456A>C	ENSP00000510501.1:p.Arg486=
ENST00000691308.1:c.829-153A>C	ENSP00000509583.1:n.829-153A>C
ENST00000448666.7:c.1456A>C MANE Select	ENSP00000410992.3:p.Arg486=
ENST00000452063.7:c.1138A>C	ENSP00000388201.2:p.Arg380=
ENST00000462443.2:c.631A>C	ENSP00000497265.1:p.Arg211=
ENST00000647723.1:c.1399A>C
ENST00000647753.1:c.*749A>C	ENSP00000497318.1:n.*749A>C
ENST00000647771.1:c.*944A>C	ENSP00000496788.1:n.*944A>C
ENST00000647915.1:c.*749A>C	ENSP00000498123.1:n.*749A>C
ENST00000648768.1:n.1713A>C
ENST00000648810.1:c.631A>C	ENSP00000496949.1:p.Arg211=
ENST00000649075.1:c.*384A>C	ENSP00000497836.1:n.*384A>C
ENST00000649601.1:c.*636A>C	ENSP00000496796.1:n.*636A>C
ENST00000649777.1:n.1665A>C
ENST00000649854.1:c.1089A>C
ENST00000650523.1:c.1231A>C	ENSP00000497143.1:p.Arg411=
ENST00000233616.8:c.1456A>C	ENSP00000233616.4:p.Arg486=
ENST00000409065.5:c.*636A>C	ENSP00000386493.1:n.*636A>C
ENST00000448666.5:c.1138A>C	ENSP00000410992.1:p.Arg380=
ENST00000452063.6:c.1138A>C	ENSP00000388201.2:p.Arg380=
ENST00000462189.1:n.1137A>C
NM_001146158.1:c.1138A>C	NP_001139630.1:p.Arg380=
NM_006302.2:c.1456A>C	NP_006293.2:p.Arg486=
NM_006302.3:c.1456A>C MANE Select	NP_006293.2:p.Arg486=
NM_001146158.2:c.1138A>C	NP_001139630.1:p.Arg380=