Canonical Allele Identifier: CA412725186

Gene: OTC

Linked Data

• MyVariant Identifiers: chrX:g.38262879T>A (hg19) ; chrX:g.38403626T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38403626T>A , CM000685.2:g.38403626T>A	GRCh38
NC_000023.10:g.38262879T>A , CM000685.1:g.38262879T>A	GRCh37
NC_000023.9:g.38147823T>A	NCBI36
NG_008471.1:g.56144T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.549T>A MANE Select	ENSP00000039007.4:p.Tyr183Ter
ENST00000643344.1:c.*299T>A	ENSP00000496606.1:n.*299T>A
ENST00000039007.4:c.549T>A	ENSP00000039007.4:p.Tyr183Ter
ENST00000465127.1:c.172-262495T>A	ENSP00000417050.1:n.172-262495T>A
ENST00000488812.1:n.586T>A
NM_000531.5:c.549T>A	NP_000522.3:p.Tyr183Ter
XM_017029556.1:c.549T>A	XP_016885045.1:p.Tyr183Ter
NM_000531.6:c.549T>A MANE Select	NP_000522.3:p.Tyr183Ter