Canonical Allele Identifier: CA412723426

Gene: OTC

Linked Data

• ClinVar Variation Id: 1724440
• ClinVar RCV Id: RCV002309708
• MyVariant Identifiers: chrX:g.38268237A>T (hg19) ; chrX:g.38408984A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38408984A>T , CM000685.2:g.38408984A>T	GRCh38
NC_000023.10:g.38268237A>T , CM000685.1:g.38268237A>T	GRCh37
NC_000023.9:g.38153181A>T	NCBI36
NG_008471.1:g.61502A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.826A>T MANE Select	ENSP00000039007.4:p.Lys276Ter
ENST00000643344.1:c.*576A>T	ENSP00000496606.1:n.*576A>T
ENST00000039007.4:c.826A>T	ENSP00000039007.4:p.Lys276Ter
ENST00000465127.1:c.172-257137A>T	ENSP00000417050.1:n.172-257137A>T
NM_000531.5:c.826A>T	NP_000522.3:p.Lys276Ter
XM_017029556.1:c.826A>T	XP_016885045.1:p.Lys276Ter
NM_000531.6:c.826A>T MANE Select	NP_000522.3:p.Lys276Ter