Canonical Allele Identifier: CA2424870734
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367115C= , CM000685.2:g.38367115C= GRCh38
NC_000023.10:g.38226368C= , CM000685.1:g.38226368C= GRCh37
NC_000023.9:g.38111312C= NCBI36
NG_008471.1:g.19633C=

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.78-176C= MANE Select ENSP00000039007.4:n.78-176C=
ENST00000643344.1:c.78-176C= ENSP00000496606.1:n.78-176C=
ENST00000039007.4:c.78-176C= ENSP00000039007.4:n.78-176C=
ENST00000465127.1:c.172-299006C= ENSP00000417050.1:n.172-299006C=
ENST00000488812.1:n.170-176C=
NM_000531.5:c.78-176C= NP_000522.3:n.78-176C=
XM_017029556.1:c.78-176C= XP_016885045.1:n.78-176C=
NM_000531.6:c.78-176C= MANE Select NP_000522.3:n.78-176C=