Canonical Allele Identifier: CA1261438271
Gene: MOGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74462339_74462340delinsTC , CM000664.2:g.74462339_74462340delinsTC GRCh38
NC_000002.11:g.74689466_74689467delinsTC , CM000664.1:g.74689466_74689467delinsTC GRCh37
NC_000002.10:g.74542974_74542975delinsTC NCBI36
NG_008922.1:g.8071_8072delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000690565.1:c.1449_1450delinsGA ENSP00000510501.1:p.Trp483=
ENST00000691308.1:c.829-160_829-159delinsGA ENSP00000509583.1:n.829-160_829-159delinsGA
ENST00000448666.7:c.1449_1450delinsGA MANE Select ENSP00000410992.3:p.Trp483=
ENST00000452063.7:c.1131_1132delinsGA ENSP00000388201.2:p.Trp377=
ENST00000462443.2:c.624_625delinsGA ENSP00000497265.1:p.Trp208=
ENST00000647723.1:c.1392_1393delinsGA
ENST00000647753.1:c.*742_*743delinsGA ENSP00000497318.1:n.*742_*743delinsGA
ENST00000647771.1:c.*937_*938delinsGA ENSP00000496788.1:n.*937_*938delinsGA
ENST00000647915.1:c.*742_*743delinsGA ENSP00000498123.1:n.*742_*743delinsGA
ENST00000648768.1:n.1706_1707delinsGA
ENST00000648810.1:c.624_625delinsGA ENSP00000496949.1:p.Trp208=
ENST00000649075.1:c.*377_*378delinsGA ENSP00000497836.1:n.*377_*378delinsGA
ENST00000649601.1:c.*629_*630delinsGA ENSP00000496796.1:n.*629_*630delinsGA
ENST00000649777.1:n.1658_1659delinsGA
ENST00000649854.1:c.1082_1083delinsGA
ENST00000650523.1:c.1224_1225delinsGA ENSP00000497143.1:p.Trp408=
ENST00000233616.8:c.1449_1450delinsGA ENSP00000233616.4:p.Trp483=
ENST00000409065.5:c.*629_*630delinsGA ENSP00000386493.1:n.*629_*630delinsGA
ENST00000448666.5:c.1131_1132delinsGA ENSP00000410992.1:p.Trp377=
ENST00000452063.6:c.1131_1132delinsGA ENSP00000388201.2:p.Trp377=
ENST00000462189.1:n.1130_1131delinsGA
NM_001146158.1:c.1131_1132delinsGA NP_001139630.1:p.Trp377=
NM_006302.2:c.1449_1450delinsGA NP_006293.2:p.Trp483=
NM_006302.3:c.1449_1450delinsGA MANE Select NP_006293.2:p.Trp483=
NM_001146158.2:c.1131_1132delinsGA NP_001139630.1:p.Trp377=