Canonical Allele Identifier: CA10385884

Gene: OTC

Linked Data

• dbSNP Id: rs772100645
• ExAC: X:38260712 C / T
• gnomAD v2: X-38260712-C-T
• gnomAD v4: X-38401459-C-T
• MyVariant Identifiers: chrX:g.38260712C>T (hg19) ; chrX:g.38401459C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38401459C>T , CM000685.2:g.38401459C>T	GRCh38
NC_000023.10:g.38260712C>T , CM000685.1:g.38260712C>T	GRCh37
NC_000023.9:g.38145656C>T	NCBI36
NG_008471.1:g.53977C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000039007.5:c.540+31C>T MANE Select	ENSP00000039007.4:n.540+31C>T
ENST00000643344.1:c.*290+31C>T	ENSP00000496606.1:n.*290+31C>T
ENST00000039007.4:c.540+31C>T	ENSP00000039007.4:n.540+31C>T
ENST00000465127.1:c.172-264662C>T	ENSP00000417050.1:n.172-264662C>T
ENST00000488812.1:n.577+31C>T
NM_000531.5:c.540+31C>T	NP_000522.3:n.540+31C>T
XM_017029556.1:c.540+31C>T	XP_016885045.1:n.540+31C>T
NM_000531.6:c.540+31C>T MANE Select	NP_000522.3:n.540+31C>T