Canonical Allele Identifier: CA412722685
Gene: OTC HGNC NCBI

Linked Data

ClinVar Variation Id: 870326
ClinVar RCV Id: RCV001089870
dbSNP Id: rs2068529566
MyVariant Identifiers: chrX:g.38268177G>T (hg19) chrX:g.38408924G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38408924G>T , CM000685.2:g.38408924G>T GRCh38
NC_000023.10:g.38268177G>T , CM000685.1:g.38268177G>T GRCh37
NC_000023.9:g.38153121G>T NCBI36
NG_008471.1:g.61442G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.766G>T MANE Select ENSP00000039007.4:p.Gly256Ter
ENST00000643344.1:c.*516G>T ENSP00000496606.1:n.*516G>T
ENST00000039007.4:c.766G>T ENSP00000039007.4:p.Gly256Ter
ENST00000465127.1:c.172-257197G>T ENSP00000417050.1:n.172-257197G>T
NM_000531.5:c.766G>T NP_000522.3:p.Gly256Ter
XM_017029556.1:c.766G>T XP_016885045.1:p.Gly256Ter
NM_000531.6:c.766G>T MANE Select NP_000522.3:p.Gly256Ter
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