Canonical Allele Identifier: CA347371055

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689171A>T (hg19) ; chr2:g.74462044A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462044A>T , CM000664.2:g.74462044A>T	GRCh38
NC_000002.11:g.74689171A>T , CM000664.1:g.74689171A>T	GRCh37
NC_000002.10:g.74542679A>T	NCBI36
NG_008922.1:g.8367T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1745T>A	ENSP00000510501.1:p.Leu582Gln
ENST00000691308.1:c.965T>A	ENSP00000509583.1:p.Leu322Gln
ENST00000448666.7:c.1745T>A MANE Select	ENSP00000410992.3:p.Leu582Gln
ENST00000452063.7:c.1427T>A	ENSP00000388201.2:p.Leu476Gln
ENST00000462443.2:c.920T>A	ENSP00000497265.1:p.Leu307Gln
ENST00000647723.1:c.1688T>A
ENST00000647753.1:c.*1038T>A	ENSP00000497318.1:n.*1038T>A
ENST00000647771.1:c.*1233T>A	ENSP00000496788.1:n.*1233T>A
ENST00000647915.1:c.*1038T>A	ENSP00000498123.1:n.*1038T>A
ENST00000648768.1:n.2002T>A
ENST00000648810.1:c.920T>A	ENSP00000496949.1:p.Leu307Gln
ENST00000649075.1:c.*673T>A	ENSP00000497836.1:n.*673T>A
ENST00000649601.1:c.*925T>A	ENSP00000496796.1:n.*925T>A
ENST00000649777.1:n.1954T>A
ENST00000649854.1:c.1378T>A
ENST00000233616.8:c.1745T>A	ENSP00000233616.4:p.Leu582Gln
ENST00000409065.5:c.*925T>A	ENSP00000386493.1:n.*925T>A
ENST00000448666.5:c.1427T>A	ENSP00000410992.1:p.Leu476Gln
ENST00000452063.6:c.1427T>A	ENSP00000388201.2:p.Leu476Gln
ENST00000462189.1:n.1426T>A
NM_001146158.1:c.1427T>A	NP_001139630.1:p.Leu476Gln
NM_006302.2:c.1745T>A	NP_006293.2:p.Leu582Gln
NM_006302.3:c.1745T>A MANE Select	NP_006293.2:p.Leu582Gln
NM_001146158.2:c.1427T>A	NP_001139630.1:p.Leu476Gln