Canonical Allele Identifier: CA2424871647
Gene: OTC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369775A= , CM000685.2:g.38369775A= GRCh38
NC_000023.10:g.38229028A= , CM000685.1:g.38229028A= GRCh37
NC_000023.9:g.38113972A= NCBI36
NG_008471.1:g.22293A=

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.217-21A= MANE Select ENSP00000039007.4:n.217-21A=
ENST00000643344.1:c.217-21A= ENSP00000496606.1:n.217-21A=
ENST00000039007.4:c.217-21A= ENSP00000039007.4:n.217-21A=
ENST00000465127.1:c.172-296346A= ENSP00000417050.1:n.172-296346A=
ENST00000488812.1:n.309-21A=
NM_000531.5:c.217-21A= NP_000522.3:n.217-21A=
XM_017029556.1:c.217-21A= XP_016885045.1:n.217-21A=
NM_000531.6:c.217-21A= MANE Select NP_000522.3:n.217-21A=
Search 100 bp 5'
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