Canonical Allele Identifier: CA347371085

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689178A>C (hg19) ; chr2:g.74462051A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462051A>C , CM000664.2:g.74462051A>C	GRCh38
NC_000002.11:g.74689178A>C , CM000664.1:g.74689178A>C	GRCh37
NC_000002.10:g.74542686A>C	NCBI36
NG_008922.1:g.8360T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1738T>G	ENSP00000510501.1:p.Ser580Ala
ENST00000691308.1:c.958T>G	ENSP00000509583.1:p.Ser320Ala
ENST00000448666.7:c.1738T>G MANE Select	ENSP00000410992.3:p.Ser580Ala
ENST00000452063.7:c.1420T>G	ENSP00000388201.2:p.Ser474Ala
ENST00000462443.2:c.913T>G	ENSP00000497265.1:p.Ser305Ala
ENST00000647723.1:c.1681T>G
ENST00000647753.1:c.*1031T>G	ENSP00000497318.1:n.*1031T>G
ENST00000647771.1:c.*1226T>G	ENSP00000496788.1:n.*1226T>G
ENST00000647915.1:c.*1031T>G	ENSP00000498123.1:n.*1031T>G
ENST00000648768.1:n.1995T>G
ENST00000648810.1:c.913T>G	ENSP00000496949.1:p.Ser305Ala
ENST00000649075.1:c.*666T>G	ENSP00000497836.1:n.*666T>G
ENST00000649601.1:c.*918T>G	ENSP00000496796.1:n.*918T>G
ENST00000649777.1:n.1947T>G
ENST00000649854.1:c.1371T>G
ENST00000233616.8:c.1738T>G	ENSP00000233616.4:p.Ser580Ala
ENST00000409065.5:c.*918T>G	ENSP00000386493.1:n.*918T>G
ENST00000448666.5:c.1420T>G	ENSP00000410992.1:p.Ser474Ala
ENST00000452063.6:c.1420T>G	ENSP00000388201.2:p.Ser474Ala
ENST00000462189.1:n.1419T>G
NM_001146158.1:c.1420T>G	NP_001139630.1:p.Ser474Ala
NM_006302.2:c.1738T>G	NP_006293.2:p.Ser580Ala
NM_006302.3:c.1738T>G MANE Select	NP_006293.2:p.Ser580Ala
NM_001146158.2:c.1420T>G	NP_001139630.1:p.Ser474Ala