Canonical Allele Identifier: CA347371138

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689189T>C (hg19) ; chr2:g.74462062T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462062T>C , CM000664.2:g.74462062T>C	GRCh38
NC_000002.11:g.74689189T>C , CM000664.1:g.74689189T>C	GRCh37
NC_000002.10:g.74542697T>C	NCBI36
NG_008922.1:g.8349A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1727A>G	ENSP00000510501.1:p.Lys576Arg
ENST00000691308.1:c.947A>G	ENSP00000509583.1:p.Lys316Arg
ENST00000448666.7:c.1727A>G MANE Select	ENSP00000410992.3:p.Lys576Arg
ENST00000452063.7:c.1409A>G	ENSP00000388201.2:p.Lys470Arg
ENST00000462443.2:c.902A>G	ENSP00000497265.1:p.Lys301Arg
ENST00000647723.1:c.1670A>G
ENST00000647753.1:c.*1020A>G	ENSP00000497318.1:n.*1020A>G
ENST00000647771.1:c.*1215A>G	ENSP00000496788.1:n.*1215A>G
ENST00000647915.1:c.*1020A>G	ENSP00000498123.1:n.*1020A>G
ENST00000648768.1:n.1984A>G
ENST00000648810.1:c.902A>G	ENSP00000496949.1:p.Lys301Arg
ENST00000649075.1:c.*655A>G	ENSP00000497836.1:n.*655A>G
ENST00000649601.1:c.*907A>G	ENSP00000496796.1:n.*907A>G
ENST00000649777.1:n.1936A>G
ENST00000649854.1:c.1360A>G
ENST00000233616.8:c.1727A>G	ENSP00000233616.4:p.Lys576Arg
ENST00000409065.5:c.*907A>G	ENSP00000386493.1:n.*907A>G
ENST00000448666.5:c.1409A>G	ENSP00000410992.1:p.Lys470Arg
ENST00000452063.6:c.1409A>G	ENSP00000388201.2:p.Lys470Arg
ENST00000462189.1:n.1408A>G
NM_001146158.1:c.1409A>G	NP_001139630.1:p.Lys470Arg
NM_006302.2:c.1727A>G	NP_006293.2:p.Lys576Arg
NM_006302.3:c.1727A>G MANE Select	NP_006293.2:p.Lys576Arg
NM_001146158.2:c.1409A>G	NP_001139630.1:p.Lys470Arg