Canonical Allele Identifier: CA412725202
Gene: OTC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38403630T>G , CM000685.2:g.38403630T>G GRCh38
NC_000023.10:g.38262883T>G , CM000685.1:g.38262883T>G GRCh37
NC_000023.9:g.38147827T>G NCBI36
NG_008471.1:g.56148T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.553T>G MANE Select ENSP00000039007.4:p.Ser185Ala
ENST00000643344.1:c.*303T>G ENSP00000496606.1:n.*303T>G
ENST00000039007.4:c.553T>G ENSP00000039007.4:p.Ser185Ala
ENST00000465127.1:c.172-262491T>G ENSP00000417050.1:n.172-262491T>G
ENST00000488812.1:n.590T>G
NM_000531.5:c.553T>G NP_000522.3:p.Ser185Ala
XM_017029556.1:c.553T>G XP_016885045.1:p.Ser185Ala
NM_000531.6:c.553T>G MANE Select NP_000522.3:p.Ser185Ala