Canonical Allele Identifier: CA347370783

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689138A>G (hg19) ; chr2:g.74462011A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462011A>G , CM000664.2:g.74462011A>G	GRCh38
NC_000002.11:g.74689138A>G , CM000664.1:g.74689138A>G	GRCh37
NC_000002.10:g.74542646A>G	NCBI36
NG_008922.1:g.8400T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1778T>C	ENSP00000510501.1:p.Val593Ala
ENST00000691308.1:c.998T>C	ENSP00000509583.1:p.Val333Ala
ENST00000448666.7:c.1778T>C MANE Select	ENSP00000410992.3:p.Val593Ala
ENST00000452063.7:c.1460T>C	ENSP00000388201.2:p.Val487Ala
ENST00000462443.2:c.953T>C	ENSP00000497265.1:p.Val318Ala
ENST00000647723.1:c.1721T>C
ENST00000647753.1:c.*1071T>C	ENSP00000497318.1:n.*1071T>C
ENST00000647771.1:c.*1266T>C	ENSP00000496788.1:n.*1266T>C
ENST00000647915.1:c.*1071T>C	ENSP00000498123.1:n.*1071T>C
ENST00000648768.1:n.2035T>C
ENST00000648810.1:c.953T>C	ENSP00000496949.1:p.Val318Ala
ENST00000649075.1:c.*706T>C	ENSP00000497836.1:n.*706T>C
ENST00000649601.1:c.*958T>C	ENSP00000496796.1:n.*958T>C
ENST00000649777.1:n.1987T>C
ENST00000649854.1:c.1411T>C
ENST00000233616.8:c.1778T>C	ENSP00000233616.4:p.Val593Ala
ENST00000409065.5:c.*958T>C	ENSP00000386493.1:n.*958T>C
ENST00000448666.5:c.1460T>C	ENSP00000410992.1:p.Val487Ala
ENST00000452063.6:c.1460T>C	ENSP00000388201.2:p.Val487Ala
ENST00000462189.1:n.1459T>C
NM_001146158.1:c.1460T>C	NP_001139630.1:p.Val487Ala
NM_006302.2:c.1778T>C	NP_006293.2:p.Val593Ala
NM_006302.3:c.1778T>C MANE Select	NP_006293.2:p.Val593Ala
NM_001146158.2:c.1460T>C	NP_001139630.1:p.Val487Ala