Canonical Allele Identifier: CA427034020

Gene: MOGS

Linked Data

• gnomAD v4: 2-74462343-G-C
• MyVariant Identifiers: chr2:g.74689470G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462343G>C , CM000664.2:g.74462343G>C	GRCh38
NC_000002.11:g.74689470G>C , CM000664.1:g.74689470G>C	GRCh37
NC_000002.10:g.74542978G>C	NCBI36
NG_008922.1:g.8068C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000690565.1:c.1446C>G	ENSP00000510501.1:p.Gly482=
ENST00000691308.1:c.829-163C>G	ENSP00000509583.1:n.829-163C>G
ENST00000448666.7:c.1446C>G MANE Select	ENSP00000410992.3:p.Gly482=
ENST00000452063.7:c.1128C>G	ENSP00000388201.2:p.Gly376=
ENST00000462443.2:c.621C>G	ENSP00000497265.1:p.Gly207=
ENST00000647723.1:c.1389C>G
ENST00000647753.1:c.*739C>G	ENSP00000497318.1:n.*739C>G
ENST00000647771.1:c.*934C>G	ENSP00000496788.1:n.*934C>G
ENST00000647915.1:c.*739C>G	ENSP00000498123.1:n.*739C>G
ENST00000648768.1:n.1703C>G
ENST00000648810.1:c.621C>G	ENSP00000496949.1:p.Gly207=
ENST00000649075.1:c.*374C>G	ENSP00000497836.1:n.*374C>G
ENST00000649601.1:c.*626C>G	ENSP00000496796.1:n.*626C>G
ENST00000649777.1:n.1655C>G
ENST00000649854.1:c.1079C>G
ENST00000650523.1:c.1221C>G	ENSP00000497143.1:p.Gly407=
ENST00000233616.8:c.1446C>G	ENSP00000233616.4:p.Gly482=
ENST00000409065.5:c.*626C>G	ENSP00000386493.1:n.*626C>G
ENST00000448666.5:c.1128C>G	ENSP00000410992.1:p.Gly376=
ENST00000452063.6:c.1128C>G	ENSP00000388201.2:p.Gly376=
ENST00000462189.1:n.1127C>G
NM_001146158.1:c.1128C>G	NP_001139630.1:p.Gly376=
NM_006302.2:c.1446C>G	NP_006293.2:p.Gly482=
NM_006302.3:c.1446C>G MANE Select	NP_006293.2:p.Gly482=
NM_001146158.2:c.1128C>G	NP_001139630.1:p.Gly376=