Canonical Allele Identifier: CA640860042
Gene: OTC HGNC NCBI

Linked Data

ClinVar Variation Id: 1458268
ClinVar RCV Id: RCV001956284
dbSNP Id: rs1488225008
gnomAD v2: X-38271101-C-T
gnomAD v4: X-38411848-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38411848C>T , CM000685.2:g.38411848C>T GRCh38
NC_000023.10:g.38271101C>T , CM000685.1:g.38271101C>T GRCh37
NC_000023.9:g.38156045C>T NCBI36
NG_008471.1:g.64366C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.868-14C>T MANE Select ENSP00000039007.4:n.868-14C>T
ENST00000643344.1:c.*618-14C>T ENSP00000496606.1:n.*618-14C>T
ENST00000039007.4:c.868-14C>T ENSP00000039007.4:n.868-14C>T
ENST00000465127.1:c.172-254273C>T ENSP00000417050.1:n.172-254273C>T
NM_000531.5:c.868-14C>T NP_000522.3:n.868-14C>T
XM_017029556.1:c.923C>T XP_016885045.1:p.Ser308Phe
NM_000531.6:c.868-14C>T MANE Select NP_000522.3:n.868-14C>T