Canonical Allele Identifier: CA1725132
Gene: MOGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74465236G>C , CM000664.2:g.74465236G>C GRCh38
NC_000002.11:g.74692363G>C , CM000664.1:g.74692363G>C GRCh37
NC_000002.10:g.74545871G>C NCBI36
NG_008922.1:g.5175C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000690565.1:c.12C>G ENSP00000510501.1:p.Gly4=
ENST00000691308.1:c.12C>G ENSP00000509583.1:p.Gly4=
ENST00000448666.7:c.12C>G MANE Select ENSP00000410992.3:p.Gly4=
ENST00000452063.7:c.-59+78C>G ENSP00000388201.2:n.-59+78C>G
ENST00000462443.2:c.-247+78C>G ENSP00000497265.1:n.-247+78C>G
ENST00000647723.1:c.10C>G
ENST00000647753.1:c.12C>G ENSP00000497318.1:p.Gly4=
ENST00000647771.1:c.12C>G ENSP00000496788.1:p.Gly4=
ENST00000647915.1:c.-59+78C>G ENSP00000498123.1:n.-59+78C>G
ENST00000648768.1:n.92C>G
ENST00000648810.1:c.-192+78C>G ENSP00000496949.1:n.-192+78C>G
ENST00000649075.1:c.12C>G ENSP00000497836.1:p.Gly4=
ENST00000649601.1:c.-59+78C>G ENSP00000496796.1:n.-59+78C>G
ENST00000649777.1:n.48C>G
ENST00000650523.1:c.12C>G ENSP00000497143.1:p.Gly4=
ENST00000233616.8:c.12C>G ENSP00000233616.4:p.Gly4=
ENST00000409065.5:c.12C>G ENSP00000386493.1:p.Gly4=
ENST00000414701.1:c.-6+78C>G ENSP00000396298.1:n.-6+78C>G
ENST00000448666.5:c.-59+78C>G ENSP00000410992.1:n.-59+78C>G
ENST00000452063.6:c.-59+78C>G ENSP00000388201.2:n.-59+78C>G
ENST00000462443.1:n.97+78C>G
ENST00000486036.1:n.165C>G
NM_001146158.1:c.-59+78C>G NP_001139630.1:n.-59+78C>G
NM_006302.2:c.12C>G NP_006293.2:p.Gly4=
NM_006302.3:c.12C>G MANE Select NP_006293.2:p.Gly4=
NM_001146158.2:c.-59+78C>G NP_001139630.1:n.-59+78C>G