Canonical Allele Identifier: CA347372459

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689473A>C (hg19) ; chr2:g.74462346A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1443T>G	ENSP00000510501.1:p.Asp481Glu
ENST00000691308.1:c.829-166T>G	ENSP00000509583.1:n.829-166T>G
ENST00000448666.7:c.1443T>G MANE Select	ENSP00000410992.3:p.Asp481Glu
ENST00000452063.7:c.1125T>G	ENSP00000388201.2:p.Asp375Glu
ENST00000462443.2:c.618T>G	ENSP00000497265.1:p.Asp206Glu
ENST00000647723.1:c.1386T>G
ENST00000647753.1:c.*736T>G	ENSP00000497318.1:n.*736T>G
ENST00000647771.1:c.*931T>G	ENSP00000496788.1:n.*931T>G
ENST00000647915.1:c.*736T>G	ENSP00000498123.1:n.*736T>G
ENST00000648768.1:n.1700T>G
ENST00000648810.1:c.618T>G	ENSP00000496949.1:p.Asp206Glu
ENST00000649075.1:c.*371T>G	ENSP00000497836.1:n.*371T>G
ENST00000649601.1:c.*623T>G	ENSP00000496796.1:n.*623T>G
ENST00000649777.1:n.1652T>G
ENST00000649854.1:c.1076T>G
ENST00000650523.1:c.1218T>G	ENSP00000497143.1:p.Asp406Glu
ENST00000233616.8:c.1443T>G	ENSP00000233616.4:p.Asp481Glu
ENST00000409065.5:c.*623T>G	ENSP00000386493.1:n.*623T>G
ENST00000448666.5:c.1125T>G	ENSP00000410992.1:p.Asp375Glu
ENST00000452063.6:c.1125T>G	ENSP00000388201.2:p.Asp375Glu
ENST00000462189.1:n.1124T>G
NM_001146158.1:c.1125T>G	NP_001139630.1:p.Asp375Glu
NM_006302.2:c.1443T>G	NP_006293.2:p.Asp481Glu
NM_006302.3:c.1443T>G MANE Select	NP_006293.2:p.Asp481Glu
NM_001146158.2:c.1125T>G	NP_001139630.1:p.Asp375Glu