Canonical Allele Identifier: CA412726677
Gene: OTC HGNC NCBI

Linked Data

ClinVar Variation Id: 803979
ClinVar RCV Id: RCV000990791
dbSNP Id: rs1602034625
MyVariant Identifiers: chrX:g.38271221C>T (hg19) chrX:g.38411968C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38411968C>T , CM000685.2:g.38411968C>T GRCh38
NC_000023.10:g.38271221C>T , CM000685.1:g.38271221C>T GRCh37
NC_000023.9:g.38156165C>T NCBI36
NG_008471.1:g.64486C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.974C>T MANE Select ENSP00000039007.4:p.Pro325Leu
ENST00000643344.1:c.*724C>T ENSP00000496606.1:n.*724C>T
ENST00000039007.4:c.974C>T ENSP00000039007.4:p.Pro325Leu
ENST00000465127.1:c.172-254153C>T ENSP00000417050.1:n.172-254153C>T
NM_000531.5:c.974C>T NP_000522.3:p.Pro325Leu
NM_000531.6:c.974C>T MANE Select NP_000522.3:p.Pro325Leu
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