Canonical Allele Identifier: CA2424871642
Gene: OTC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369752T= , CM000685.2:g.38369752T= GRCh38
NC_000023.10:g.38229005T= , CM000685.1:g.38229005T= GRCh37
NC_000023.9:g.38113949T= NCBI36
NG_008471.1:g.22270T=

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.217-44T= MANE Select ENSP00000039007.4:n.217-44T=
ENST00000643344.1:c.217-44T= ENSP00000496606.1:n.217-44T=
ENST00000039007.4:c.217-44T= ENSP00000039007.4:n.217-44T=
ENST00000465127.1:c.172-296369T= ENSP00000417050.1:n.172-296369T=
ENST00000488812.1:n.309-44T=
NM_000531.5:c.217-44T= NP_000522.3:n.217-44T=
XM_017029556.1:c.217-44T= XP_016885045.1:n.217-44T=
NM_000531.6:c.217-44T= MANE Select NP_000522.3:n.217-44T=
Search 100 bp 5'
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