Canonical Allele Identifier: CA347370758

Gene: MOGS

Linked Data

• dbSNP Id: rs1671925611
• MyVariant Identifiers: chr2:g.74689135G>A (hg19) ; chr2:g.74462008G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462008G>A , CM000664.2:g.74462008G>A	GRCh38
NC_000002.11:g.74689135G>A , CM000664.1:g.74689135G>A	GRCh37
NC_000002.10:g.74542643G>A	NCBI36
NG_008922.1:g.8403C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1781C>T	ENSP00000510501.1:p.Thr594Ile
ENST00000691308.1:c.1001C>T	ENSP00000509583.1:p.Thr334Ile
ENST00000448666.7:c.1781C>T MANE Select	ENSP00000410992.3:p.Thr594Ile
ENST00000452063.7:c.1463C>T	ENSP00000388201.2:p.Thr488Ile
ENST00000462443.2:c.956C>T	ENSP00000497265.1:p.Thr319Ile
ENST00000647723.1:c.1724C>T
ENST00000647753.1:c.*1074C>T	ENSP00000497318.1:n.*1074C>T
ENST00000647771.1:c.*1269C>T	ENSP00000496788.1:n.*1269C>T
ENST00000647915.1:c.*1074C>T	ENSP00000498123.1:n.*1074C>T
ENST00000648768.1:n.2038C>T
ENST00000648810.1:c.956C>T	ENSP00000496949.1:p.Thr319Ile
ENST00000649075.1:c.*709C>T	ENSP00000497836.1:n.*709C>T
ENST00000649601.1:c.*961C>T	ENSP00000496796.1:n.*961C>T
ENST00000649777.1:n.1990C>T
ENST00000649854.1:c.1414C>T
ENST00000233616.8:c.1781C>T	ENSP00000233616.4:p.Thr594Ile
ENST00000409065.5:c.*961C>T	ENSP00000386493.1:n.*961C>T
ENST00000448666.5:c.1463C>T	ENSP00000410992.1:p.Thr488Ile
ENST00000452063.6:c.1463C>T	ENSP00000388201.2:p.Thr488Ile
ENST00000462189.1:n.1462C>T
NM_001146158.1:c.1463C>T	NP_001139630.1:p.Thr488Ile
NM_006302.2:c.1781C>T	NP_006293.2:p.Thr594Ile
NM_006302.3:c.1781C>T MANE Select	NP_006293.2:p.Thr594Ile
NM_001146158.2:c.1463C>T	NP_001139630.1:p.Thr488Ile