Canonical Allele Identifier: CA347370692

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689127G>A (hg19) ; chr2:g.74462000G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462000G>A , CM000664.2:g.74462000G>A	GRCh38
NC_000002.11:g.74689127G>A , CM000664.1:g.74689127G>A	GRCh37
NC_000002.10:g.74542635G>A	NCBI36
NG_008922.1:g.8411C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1789C>T	ENSP00000510501.1:p.His597Tyr
ENST00000691308.1:c.1009C>T	ENSP00000509583.1:p.His337Tyr
ENST00000448666.7:c.1789C>T MANE Select	ENSP00000410992.3:p.His597Tyr
ENST00000452063.7:c.1471C>T	ENSP00000388201.2:p.His491Tyr
ENST00000462443.2:c.964C>T	ENSP00000497265.1:p.His322Tyr
ENST00000647723.1:c.1732C>T
ENST00000647753.1:c.*1082C>T	ENSP00000497318.1:n.*1082C>T
ENST00000647771.1:c.*1277C>T	ENSP00000496788.1:n.*1277C>T
ENST00000647915.1:c.*1082C>T	ENSP00000498123.1:n.*1082C>T
ENST00000648768.1:n.2046C>T
ENST00000648810.1:c.964C>T	ENSP00000496949.1:p.His322Tyr
ENST00000649075.1:c.*717C>T	ENSP00000497836.1:n.*717C>T
ENST00000649601.1:c.*969C>T	ENSP00000496796.1:n.*969C>T
ENST00000649777.1:n.1998C>T
ENST00000649854.1:c.1422C>T
ENST00000233616.8:c.1789C>T	ENSP00000233616.4:p.His597Tyr
ENST00000409065.5:c.*969C>T	ENSP00000386493.1:n.*969C>T
ENST00000448666.5:c.1471C>T	ENSP00000410992.1:p.His491Tyr
ENST00000452063.6:c.1471C>T	ENSP00000388201.2:p.His491Tyr
ENST00000462189.1:n.1470C>T
NM_001146158.1:c.1471C>T	NP_001139630.1:p.His491Tyr
NM_006302.2:c.1789C>T	NP_006293.2:p.His597Tyr
NM_006302.3:c.1789C>T MANE Select	NP_006293.2:p.His597Tyr
NM_001146158.2:c.1471C>T	NP_001139630.1:p.His491Tyr