Canonical Allele Identifier: CA347371959

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689372A>T (hg19) ; chr2:g.74462245A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462245A>T , CM000664.2:g.74462245A>T	GRCh38
NC_000002.11:g.74689372A>T , CM000664.1:g.74689372A>T	GRCh37
NC_000002.10:g.74542880A>T	NCBI36
NG_008922.1:g.8166T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1544T>A	ENSP00000510501.1:p.Leu515Gln
ENST00000691308.1:c.829-65T>A	ENSP00000509583.1:n.829-65T>A
ENST00000448666.7:c.1544T>A MANE Select	ENSP00000410992.3:p.Leu515Gln
ENST00000452063.7:c.1226T>A	ENSP00000388201.2:p.Leu409Gln
ENST00000462443.2:c.719T>A	ENSP00000497265.1:p.Leu240Gln
ENST00000647723.1:c.1487T>A
ENST00000647753.1:c.*837T>A	ENSP00000497318.1:n.*837T>A
ENST00000647771.1:c.*1032T>A	ENSP00000496788.1:n.*1032T>A
ENST00000647915.1:c.*837T>A	ENSP00000498123.1:n.*837T>A
ENST00000648768.1:n.1801T>A
ENST00000648810.1:c.719T>A	ENSP00000496949.1:p.Leu240Gln
ENST00000649075.1:c.*472T>A	ENSP00000497836.1:n.*472T>A
ENST00000649601.1:c.*724T>A	ENSP00000496796.1:n.*724T>A
ENST00000649777.1:n.1753T>A
ENST00000649854.1:c.1177T>A
ENST00000233616.8:c.1544T>A	ENSP00000233616.4:p.Leu515Gln
ENST00000409065.5:c.*724T>A	ENSP00000386493.1:n.*724T>A
ENST00000448666.5:c.1226T>A	ENSP00000410992.1:p.Leu409Gln
ENST00000452063.6:c.1226T>A	ENSP00000388201.2:p.Leu409Gln
ENST00000462189.1:n.1225T>A
NM_001146158.1:c.1226T>A	NP_001139630.1:p.Leu409Gln
NM_006302.2:c.1544T>A	NP_006293.2:p.Leu515Gln
NM_006302.3:c.1544T>A MANE Select	NP_006293.2:p.Leu515Gln
NM_001146158.2:c.1226T>A	NP_001139630.1:p.Leu409Gln