Canonical Allele Identifier: CA412716847

Gene: OTC

Linked Data

• MyVariant Identifiers: chrX:g.38229068G>T (hg19) ; chrX:g.38369815G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38369815G>T , CM000685.2:g.38369815G>T	GRCh38
NC_000023.10:g.38229068G>T , CM000685.1:g.38229068G>T	GRCh37
NC_000023.9:g.38114012G>T	NCBI36
NG_008471.1:g.22333G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.236G>T MANE Select	ENSP00000039007.4:p.Gly79Val
ENST00000643344.1:c.236G>T	ENSP00000496606.1:p.Gly79Val
ENST00000039007.4:c.236G>T	ENSP00000039007.4:p.Gly79Val
ENST00000465127.1:c.172-296306G>T	ENSP00000417050.1:n.172-296306G>T
ENST00000488812.1:n.328G>T
NM_000531.5:c.236G>T	NP_000522.3:p.Gly79Val
XM_017029556.1:c.236G>T	XP_016885045.1:p.Gly79Val
NM_000531.6:c.236G>T MANE Select	NP_000522.3:p.Gly79Val