Canonical Allele Identifier: CA2424882780
Gene: OTC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38403817G= , CM000685.2:g.38403817G= GRCh38
NC_000023.10:g.38263070G= , CM000685.1:g.38263070G= GRCh37
NC_000023.9:g.38148014G= NCBI36
NG_008471.1:g.56335G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.663+77G= MANE Select ENSP00000039007.4:n.663+77G=
ENST00000643344.1:c.*413+77G= ENSP00000496606.1:n.*413+77G=
ENST00000039007.4:c.663+77G= ENSP00000039007.4:n.663+77G=
ENST00000465127.1:c.172-262304G= ENSP00000417050.1:n.172-262304G=
NM_000531.5:c.663+77G= NP_000522.3:n.663+77G=
XM_017029556.1:c.663+77G= XP_016885045.1:n.663+77G=
NM_000531.6:c.663+77G= MANE Select NP_000522.3:n.663+77G=
Search 100 bp 5'
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