Canonical Allele Identifier: CA2424866354
Gene: OTC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38352668A= , CM000685.2:g.38352668A= GRCh38
NC_000023.10:g.38211921A= , CM000685.1:g.38211921A= GRCh37
NC_000023.9:g.38096865A= NCBI36
NG_008471.1:g.5186A=

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.-29A= MANE Select ENSP00000039007.4:n.-29A=
ENST00000643344.1:c.-29A= ENSP00000496606.1:n.-29A=
ENST00000039007.4:c.-29A= ENSP00000039007.4:n.-29A=
ENST00000465127.1:c.172-313453A= ENSP00000417050.1:n.172-313453A=
ENST00000488812.1:n.64A=
NM_000531.5:c.-29A= NP_000522.3:n.-29A=
XM_017029556.1:c.-29A= XP_016885045.1:n.-29A=
NM_000531.6:c.-29A= MANE Select NP_000522.3:n.-29A=
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