Canonical Allele Identifier: CA10385780
Gene: OTC HGNC NCBI

Linked Data

dbSNP Id: rs750152681

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367260A>G , CM000685.2:g.38367260A>G GRCh38
NC_000023.10:g.38226513A>G , CM000685.1:g.38226513A>G GRCh37
NC_000023.9:g.38111457A>G NCBI36
NG_008471.1:g.19778A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.78-31A>G MANE Select ENSP00000039007.4:n.78-31A>G
ENST00000643344.1:c.78-31A>G ENSP00000496606.1:n.78-31A>G
ENST00000039007.4:c.78-31A>G ENSP00000039007.4:n.78-31A>G
ENST00000465127.1:c.172-298861A>G ENSP00000417050.1:n.172-298861A>G
ENST00000488812.1:n.170-31A>G
NM_000531.5:c.78-31A>G NP_000522.3:n.78-31A>G
XM_017029556.1:c.78-31A>G XP_016885045.1:n.78-31A>G
NM_000531.6:c.78-31A>G MANE Select NP_000522.3:n.78-31A>G