Canonical Allele Identifier: CA412725924
Gene: OTC HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38271160C>A (hg19) chrX:g.38411907C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38411907C>A , CM000685.2:g.38411907C>A GRCh38
NC_000023.10:g.38271160C>A , CM000685.1:g.38271160C>A GRCh37
NC_000023.9:g.38156104C>A NCBI36
NG_008471.1:g.64425C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.913C>A MANE Select ENSP00000039007.4:p.Pro305Thr
ENST00000643344.1:c.*663C>A ENSP00000496606.1:n.*663C>A
ENST00000039007.4:c.913C>A ENSP00000039007.4:p.Pro305Thr
ENST00000465127.1:c.172-254214C>A ENSP00000417050.1:n.172-254214C>A
NM_000531.5:c.913C>A NP_000522.3:p.Pro305Thr
NM_000531.6:c.913C>A MANE Select NP_000522.3:p.Pro305Thr
Search 100 bp 5'
Search 100 bp 3'