Canonical Allele Identifier: CA2424885184
Gene: OTC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38411825T= , CM000685.2:g.38411825T= GRCh38
NC_000023.10:g.38271078T= , CM000685.1:g.38271078T= GRCh37
NC_000023.9:g.38156022T= NCBI36
NG_008471.1:g.64343T=

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.868-37T= MANE Select ENSP00000039007.4:n.868-37T=
ENST00000643344.1:c.*618-37T= ENSP00000496606.1:n.*618-37T=
ENST00000039007.4:c.868-37T= ENSP00000039007.4:n.868-37T=
ENST00000465127.1:c.172-254296T= ENSP00000417050.1:n.172-254296T=
NM_000531.5:c.868-37T= NP_000522.3:n.868-37T=
XM_017029556.1:c.900T= XP_016885045.1:p.Tyr300=
NM_000531.6:c.868-37T= MANE Select NP_000522.3:n.868-37T=
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