Canonical Allele Identifier: CA347370943

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689160G>C (hg19) ; chr2:g.74462033G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462033G>C , CM000664.2:g.74462033G>C	GRCh38
NC_000002.11:g.74689160G>C , CM000664.1:g.74689160G>C	GRCh37
NC_000002.10:g.74542668G>C	NCBI36
NG_008922.1:g.8378C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1756C>G	ENSP00000510501.1:p.Pro586Ala
ENST00000691308.1:c.976C>G	ENSP00000509583.1:p.Pro326Ala
ENST00000448666.7:c.1756C>G MANE Select	ENSP00000410992.3:p.Pro586Ala
ENST00000452063.7:c.1438C>G	ENSP00000388201.2:p.Pro480Ala
ENST00000462443.2:c.931C>G	ENSP00000497265.1:p.Pro311Ala
ENST00000647723.1:c.1699C>G
ENST00000647753.1:c.*1049C>G	ENSP00000497318.1:n.*1049C>G
ENST00000647771.1:c.*1244C>G	ENSP00000496788.1:n.*1244C>G
ENST00000647915.1:c.*1049C>G	ENSP00000498123.1:n.*1049C>G
ENST00000648768.1:n.2013C>G
ENST00000648810.1:c.931C>G	ENSP00000496949.1:p.Pro311Ala
ENST00000649075.1:c.*684C>G	ENSP00000497836.1:n.*684C>G
ENST00000649601.1:c.*936C>G	ENSP00000496796.1:n.*936C>G
ENST00000649777.1:n.1965C>G
ENST00000649854.1:c.1389C>G
ENST00000233616.8:c.1756C>G	ENSP00000233616.4:p.Pro586Ala
ENST00000409065.5:c.*936C>G	ENSP00000386493.1:n.*936C>G
ENST00000448666.5:c.1438C>G	ENSP00000410992.1:p.Pro480Ala
ENST00000452063.6:c.1438C>G	ENSP00000388201.2:p.Pro480Ala
ENST00000462189.1:n.1437C>G
NM_001146158.1:c.1438C>G	NP_001139630.1:p.Pro480Ala
NM_006302.2:c.1756C>G	NP_006293.2:p.Pro586Ala
NM_006302.3:c.1756C>G MANE Select	NP_006293.2:p.Pro586Ala
NM_001146158.2:c.1438C>G	NP_001139630.1:p.Pro480Ala