Canonical Allele Identifier: CA2424881905
Gene: OTC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38401450A= , CM000685.2:g.38401450A= GRCh38
NC_000023.10:g.38260703A= , CM000685.1:g.38260703A= GRCh37
NC_000023.9:g.38145647A= NCBI36
NG_008471.1:g.53968A=

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.540+22A= MANE Select ENSP00000039007.4:n.540+22A=
ENST00000643344.1:c.*290+22A= ENSP00000496606.1:n.*290+22A=
ENST00000039007.4:c.540+22A= ENSP00000039007.4:n.540+22A=
ENST00000465127.1:c.172-264671A= ENSP00000417050.1:n.172-264671A=
ENST00000488812.1:n.577+22A=
NM_000531.5:c.540+22A= NP_000522.3:n.540+22A=
XM_017029556.1:c.540+22A= XP_016885045.1:n.540+22A=
NM_000531.6:c.540+22A= MANE Select NP_000522.3:n.540+22A=
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