Canonical Allele Identifier: CA2424870753

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38367174_38367178delinsCAAAA , CM000685.2:g.38367174_38367178delinsCAAAA	GRCh38
NC_000023.10:g.38226427_38226431delinsCAAAA , CM000685.1:g.38226427_38226431delinsCAAAA	GRCh37
NC_000023.9:g.38111371_38111375delinsCAAAA	NCBI36
NG_008471.1:g.19692_19696delinsCAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.78-117_78-113delinsCAAAA MANE Select	ENSP00000039007.4:n.78-117_78-113delinsCAAAA
ENST00000643344.1:c.78-117_78-113delinsCAAAA	ENSP00000496606.1:n.78-117_78-113delinsCAAAA
ENST00000039007.4:c.78-117_78-113delinsCAAAA	ENSP00000039007.4:n.78-117_78-113delinsCAAAA
ENST00000465127.1:c.172-298947_172-298943delinsCAAAA	ENSP00000417050.1:n.172-298947_172-298943delinsCAAAA
ENST00000488812.1:n.170-117_170-113delinsCAAAA
NM_000531.5:c.78-117_78-113delinsCAAAA	NP_000522.3:n.78-117_78-113delinsCAAAA
XM_017029556.1:c.78-117_78-113delinsCAAAA	XP_016885045.1:n.78-117_78-113delinsCAAAA
NM_000531.6:c.78-117_78-113delinsCAAAA MANE Select	NP_000522.3:n.78-117_78-113delinsCAAAA