Canonical Allele Identifier: CA2424875276
Gene: OTC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38381398_38381400delinsGGT , CM000685.2:g.38381398_38381400delinsGGT GRCh38
NC_000023.10:g.38240651_38240653delinsGGT , CM000685.1:g.38240651_38240653delinsGGT GRCh37
NC_000023.9:g.38125595_38125597delinsGGT NCBI36
NG_008471.1:g.33916_33918delinsGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.355_357delinsGGT MANE Select ENSP00000039007.4:p.Gly119=
ENST00000643344.1:c.*105_*107delinsGGT ENSP00000496606.1:n.*105_*107delinsGGT
ENST00000039007.4:c.355_357delinsGGT ENSP00000039007.4:p.Gly119=
ENST00000465127.1:c.172-284723_172-284721delinsGGT ENSP00000417050.1:n.172-284723_172-284721delinsGGT
ENST00000488812.1:n.392_394delinsGGT
NM_000531.5:c.355_357delinsGGT NP_000522.3:p.Gly119=
XM_017029556.1:c.355_357delinsGGT XP_016885045.1:p.Gly119=
NM_000531.6:c.355_357delinsGGT MANE Select NP_000522.3:p.Gly119=
Search 100 bp 5'
Search 100 bp 3'