Canonical Allele Identifier: CA2424871652
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369793T= , CM000685.2:g.38369793T= GRCh38
NC_000023.10:g.38229046T= , CM000685.1:g.38229046T= GRCh37
NC_000023.9:g.38113990T= NCBI36
NG_008471.1:g.22311T=

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.217-3T= MANE Select ENSP00000039007.4:n.217-3T=
ENST00000643344.1:c.217-3T= ENSP00000496606.1:n.217-3T=
ENST00000039007.4:c.217-3T= ENSP00000039007.4:n.217-3T=
ENST00000465127.1:c.172-296328T= ENSP00000417050.1:n.172-296328T=
ENST00000488812.1:n.309-3T=
NM_000531.5:c.217-3T= NP_000522.3:n.217-3T=
XM_017029556.1:c.217-3T= XP_016885045.1:n.217-3T=
NM_000531.6:c.217-3T= MANE Select NP_000522.3:n.217-3T=