Canonical Allele Identifier: CA347371919

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689363G>C (hg19) ; chr2:g.74462236G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462236G>C , CM000664.2:g.74462236G>C	GRCh38
NC_000002.11:g.74689363G>C , CM000664.1:g.74689363G>C	GRCh37
NC_000002.10:g.74542871G>C	NCBI36
NG_008922.1:g.8175C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1553C>G	ENSP00000510501.1:p.Pro518Arg
ENST00000691308.1:c.829-56C>G	ENSP00000509583.1:n.829-56C>G
ENST00000448666.7:c.1553C>G MANE Select	ENSP00000410992.3:p.Pro518Arg
ENST00000452063.7:c.1235C>G	ENSP00000388201.2:p.Pro412Arg
ENST00000462443.2:c.728C>G	ENSP00000497265.1:p.Pro243Arg
ENST00000647723.1:c.1496C>G
ENST00000647753.1:c.*846C>G	ENSP00000497318.1:n.*846C>G
ENST00000647771.1:c.*1041C>G	ENSP00000496788.1:n.*1041C>G
ENST00000647915.1:c.*846C>G	ENSP00000498123.1:n.*846C>G
ENST00000648768.1:n.1810C>G
ENST00000648810.1:c.728C>G	ENSP00000496949.1:p.Pro243Arg
ENST00000649075.1:c.*481C>G	ENSP00000497836.1:n.*481C>G
ENST00000649601.1:c.*733C>G	ENSP00000496796.1:n.*733C>G
ENST00000649777.1:n.1762C>G
ENST00000649854.1:c.1186C>G
ENST00000233616.8:c.1553C>G	ENSP00000233616.4:p.Pro518Arg
ENST00000409065.5:c.*733C>G	ENSP00000386493.1:n.*733C>G
ENST00000448666.5:c.1235C>G	ENSP00000410992.1:p.Pro412Arg
ENST00000452063.6:c.1235C>G	ENSP00000388201.2:p.Pro412Arg
ENST00000462189.1:n.1234C>G
NM_001146158.1:c.1235C>G	NP_001139630.1:p.Pro412Arg
NM_006302.2:c.1553C>G	NP_006293.2:p.Pro518Arg
NM_006302.3:c.1553C>G MANE Select	NP_006293.2:p.Pro518Arg
NM_001146158.2:c.1235C>G	NP_001139630.1:p.Pro412Arg