Canonical Allele Identifier: CA2424870899
Gene: OTC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367545A= , CM000685.2:g.38367545A= GRCh38
NC_000023.10:g.38226798A= , CM000685.1:g.38226798A= GRCh37
NC_000023.9:g.38111742A= NCBI36
NG_008471.1:g.20063A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.216+116A= MANE Select ENSP00000039007.4:n.216+116A=
ENST00000643344.1:c.216+116A= ENSP00000496606.1:n.216+116A=
ENST00000039007.4:c.216+116A= ENSP00000039007.4:n.216+116A=
ENST00000465127.1:c.172-298576A= ENSP00000417050.1:n.172-298576A=
ENST00000488812.1:n.308+116A=
NM_000531.5:c.216+116A= NP_000522.3:n.216+116A=
XM_017029556.1:c.216+116A= XP_016885045.1:n.216+116A=
NM_000531.6:c.216+116A= MANE Select NP_000522.3:n.216+116A=
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