Canonical Allele Identifier: CA2579584741
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369793_38369794del , CM000685.2:g.38369793_38369794del GRCh38
NC_000023.10:g.38229046_38229047del , CM000685.1:g.38229046_38229047del GRCh37
NC_000023.9:g.38113990_38113991del NCBI36
NG_008471.1:g.22311_22312del

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.217-3_217-2del MANE Select ENSP00000039007.4:n.217-3_217-2del
ENST00000643344.1:c.217-3_217-2del ENSP00000496606.1:n.217-3_217-2del
ENST00000039007.4:c.217-3_217-2del ENSP00000039007.4:n.217-3_217-2del
ENST00000465127.1:c.172-296328_172-296327del ENSP00000417050.1:n.172-296328_172-296327...
ENST00000488812.1:n.309-3_309-2del
NM_000531.5:c.217-3_217-2del NP_000522.3:n.217-3_217-2del
XM_017029556.1:c.217-3_217-2del XP_016885045.1:n.217-3_217-2del
NM_000531.6:c.217-3_217-2del MANE Select NP_000522.3:n.217-3_217-2del