Canonical Allele Identifier: CA2838139630
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367420_38369805del , CM000685.2:g.38367420_38369805del GRCh38
NC_000023.10:g.38226673_38229058del , CM000685.1:g.38226673_38229058del GRCh37
NC_000023.9:g.38111617_38114002del NCBI36
NG_008471.1:g.19938_22323del

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.207_226del
ENST00000643344.1:c.207_226del
ENST00000039007.4:c.207_226del
ENST00000465127.1:c.172-298701_172-296316del ENSP00000417050.1:n.172-298701_172-296316del
ENST00000488812.1:n.299_318del
NM_000531.5:c.207_226del
XM_017029556.1:c.207_226del
NM_000531.6:c.207_226del