Canonical Allele Identifier: CA347371939

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689366A>T (hg19) ; chr2:g.74462239A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462239A>T , CM000664.2:g.74462239A>T	GRCh38
NC_000002.11:g.74689366A>T , CM000664.1:g.74689366A>T	GRCh37
NC_000002.10:g.74542874A>T	NCBI36
NG_008922.1:g.8172T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000690565.1:c.1550T>A	ENSP00000510501.1:p.Leu517Ter
ENST00000691308.1:c.829-59T>A	ENSP00000509583.1:n.829-59T>A
ENST00000448666.7:c.1550T>A MANE Select	ENSP00000410992.3:p.Leu517Ter
ENST00000452063.7:c.1232T>A	ENSP00000388201.2:p.Leu411Ter
ENST00000462443.2:c.725T>A	ENSP00000497265.1:p.Leu242Ter
ENST00000647723.1:c.1493T>A
ENST00000647753.1:c.*843T>A	ENSP00000497318.1:n.*843T>A
ENST00000647771.1:c.*1038T>A	ENSP00000496788.1:n.*1038T>A
ENST00000647915.1:c.*843T>A	ENSP00000498123.1:n.*843T>A
ENST00000648768.1:n.1807T>A
ENST00000648810.1:c.725T>A	ENSP00000496949.1:p.Leu242Ter
ENST00000649075.1:c.*478T>A	ENSP00000497836.1:n.*478T>A
ENST00000649601.1:c.*730T>A	ENSP00000496796.1:n.*730T>A
ENST00000649777.1:n.1759T>A
ENST00000649854.1:c.1183T>A
ENST00000233616.8:c.1550T>A	ENSP00000233616.4:p.Leu517Ter
ENST00000409065.5:c.*730T>A	ENSP00000386493.1:n.*730T>A
ENST00000448666.5:c.1232T>A	ENSP00000410992.1:p.Leu411Ter
ENST00000452063.6:c.1232T>A	ENSP00000388201.2:p.Leu411Ter
ENST00000462189.1:n.1231T>A
NM_001146158.1:c.1232T>A	NP_001139630.1:p.Leu411Ter
NM_006302.2:c.1550T>A	NP_006293.2:p.Leu517Ter
NM_006302.3:c.1550T>A MANE Select	NP_006293.2:p.Leu517Ter
NM_001146158.2:c.1232T>A	NP_001139630.1:p.Leu411Ter