Canonical Allele Identifier: CA2424870746
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367156C= , CM000685.2:g.38367156C= GRCh38
NC_000023.10:g.38226409C= , CM000685.1:g.38226409C= GRCh37
NC_000023.9:g.38111353C= NCBI36
NG_008471.1:g.19674C=

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.78-135C= MANE Select ENSP00000039007.4:n.78-135C=
ENST00000643344.1:c.78-135C= ENSP00000496606.1:n.78-135C=
ENST00000039007.4:c.78-135C= ENSP00000039007.4:n.78-135C=
ENST00000465127.1:c.172-298965C= ENSP00000417050.1:n.172-298965C=
ENST00000488812.1:n.170-135C=
NM_000531.5:c.78-135C= NP_000522.3:n.78-135C=
XM_017029556.1:c.78-135C= XP_016885045.1:n.78-135C=
NM_000531.6:c.78-135C= MANE Select NP_000522.3:n.78-135C=