Canonical Allele Identifier: CA224562
Gene: OTC HGNC NCBI

Linked Data

ClinVar Variation Id: 97174
dbSNP Id: rs72554355

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38381407_38381408insTT , CM000685.2:g.38381407_38381408insTT GRCh38
NC_000023.10:g.38240660_38240661insTT , CM000685.1:g.38240660_38240661insTT GRCh37
NC_000023.9:g.38125604_38125605insTT NCBI36
NG_008471.1:g.33925_33926insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.364_365insTT MANE Select ENSP00000039007.4:p.Glu122ValfsTer?
ENST00000643344.1:c.*114_*115insTT ENSP00000496606.1:n.*114_*115insTT
ENST00000039007.4:c.364_365insTT ENSP00000039007.4:p.Glu122ValfsTer?
ENST00000465127.1:c.172-284714_172-284713insTT ENSP00000417050.1:n.172-284714_172-284713insTT
ENST00000488812.1:n.401_402insTT
NM_000531.5:c.364_365insTT NP_000522.3:p.Glu122ValfsTer?
XM_017029556.1:c.364_365insTT XP_016885045.1:p.Glu122ValfsTer?
NM_000531.6:c.364_365insTT MANE Select NP_000522.3:p.Glu122ValfsTer?