Canonical Allele Identifier: CA2424870731
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367106_38367107delinsAG , CM000685.2:g.38367106_38367107delinsAG GRCh38
NC_000023.10:g.38226359_38226360delinsAG , CM000685.1:g.38226359_38226360delinsAG GRCh37
NC_000023.9:g.38111303_38111304delinsAG NCBI36
NG_008471.1:g.19624_19625delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.78-185_78-184delinsAG MANE Select ENSP00000039007.4:n.78-185_78-184delinsAG...
ENST00000643344.1:c.78-185_78-184delinsAG ENSP00000496606.1:n.78-185_78-184delinsAG...
ENST00000039007.4:c.78-185_78-184delinsAG ENSP00000039007.4:n.78-185_78-184delinsAG...
ENST00000465127.1:c.172-299015_172-299014delinsAG ENSP00000417050.1:n.172-299015_172-299014...
ENST00000488812.1:n.170-185_170-184delinsAG
NM_000531.5:c.78-185_78-184delinsAG NP_000522.3:n.78-185_78-184delinsAG
XM_017029556.1:c.78-185_78-184delinsAG XP_016885045.1:n.78-185_78-184delinsAG
NM_000531.6:c.78-185_78-184delinsAG MANE Select NP_000522.3:n.78-185_78-184delinsAG