Canonical Allele Identifier: CA347372432

Gene: MOGS

Linked Data

• gnomAD v4: 2-74462342-A-C
• MyVariant Identifiers: chr2:g.74689469A>C (hg19) ; chr2:g.74462342A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462342A>C , CM000664.2:g.74462342A>C	GRCh38
NC_000002.11:g.74689469A>C , CM000664.1:g.74689469A>C	GRCh37
NC_000002.10:g.74542977A>C	NCBI36
NG_008922.1:g.8069T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000690565.1:c.1447T>G	ENSP00000510501.1:p.Trp483Gly
ENST00000691308.1:c.829-162T>G	ENSP00000509583.1:n.829-162T>G
ENST00000448666.7:c.1447T>G MANE Select	ENSP00000410992.3:p.Trp483Gly
ENST00000452063.7:c.1129T>G	ENSP00000388201.2:p.Trp377Gly
ENST00000462443.2:c.622T>G	ENSP00000497265.1:p.Trp208Gly
ENST00000647723.1:c.1390T>G
ENST00000647753.1:c.*740T>G	ENSP00000497318.1:n.*740T>G
ENST00000647771.1:c.*935T>G	ENSP00000496788.1:n.*935T>G
ENST00000647915.1:c.*740T>G	ENSP00000498123.1:n.*740T>G
ENST00000648768.1:n.1704T>G
ENST00000648810.1:c.622T>G	ENSP00000496949.1:p.Trp208Gly
ENST00000649075.1:c.*375T>G	ENSP00000497836.1:n.*375T>G
ENST00000649601.1:c.*627T>G	ENSP00000496796.1:n.*627T>G
ENST00000649777.1:n.1656T>G
ENST00000649854.1:c.1080T>G
ENST00000650523.1:c.1222T>G	ENSP00000497143.1:p.Trp408Gly
ENST00000233616.8:c.1447T>G	ENSP00000233616.4:p.Trp483Gly
ENST00000409065.5:c.*627T>G	ENSP00000386493.1:n.*627T>G
ENST00000448666.5:c.1129T>G	ENSP00000410992.1:p.Trp377Gly
ENST00000452063.6:c.1129T>G	ENSP00000388201.2:p.Trp377Gly
ENST00000462189.1:n.1128T>G
NM_001146158.1:c.1129T>G	NP_001139630.1:p.Trp377Gly
NM_006302.2:c.1447T>G	NP_006293.2:p.Trp483Gly
NM_006302.3:c.1447T>G MANE Select	NP_006293.2:p.Trp483Gly
NM_001146158.2:c.1129T>G	NP_001139630.1:p.Trp377Gly