Canonical Allele Identifier: CA327927458

Gene: OTC

Linked Data

• dbSNP Id: rs185020323
• gnomAD v2: X-38229521-G-A
• gnomAD v3: X-38370268-G-A
• gnomAD v4: X-38370268-G-A
• MyVariant Identifiers: chrX:g.38229521G>A (hg19) ; chrX:g.38370268G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38370268G>A , CM000685.2:g.38370268G>A	GRCh38
NC_000023.10:g.38229521G>A , CM000685.1:g.38229521G>A	GRCh37
NC_000023.9:g.38114465G>A	NCBI36
NG_008471.1:g.22786G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.298+391G>A MANE Select	ENSP00000039007.4:n.298+391G>A
ENST00000643344.1:c.298+391G>A	ENSP00000496606.1:n.298+391G>A
ENST00000039007.4:c.298+391G>A	ENSP00000039007.4:n.298+391G>A
ENST00000465127.1:c.172-295853G>A	ENSP00000417050.1:n.172-295853G>A
ENST00000488812.1:n.353+428G>A
NM_000531.5:c.298+391G>A	NP_000522.3:n.298+391G>A
XM_017029556.1:c.298+391G>A	XP_016885045.1:n.298+391G>A
NM_000531.6:c.298+391G>A MANE Select	NP_000522.3:n.298+391G>A