Canonical Allele Identifier: CA2693442165

Gene: OTC

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38367188_38367189insT , CM000685.2:g.38367188_38367189insT	GRCh38
NC_000023.10:g.38226441_38226442insT , CM000685.1:g.38226441_38226442insT	GRCh37
NC_000023.9:g.38111385_38111386insT	NCBI36
NG_008471.1:g.19706_19707insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.78-103_78-102insT MANE Select	ENSP00000039007.4:n.78-103_78-102insT
ENST00000643344.1:c.78-103_78-102insT	ENSP00000496606.1:n.78-103_78-102insT
ENST00000039007.4:c.78-103_78-102insT	ENSP00000039007.4:n.78-103_78-102insT
ENST00000465127.1:c.172-298933_172-298932insT	ENSP00000417050.1:n.172-298933_172-298932insT
ENST00000488812.1:n.170-103_170-102insT
NM_000531.5:c.78-103_78-102insT	NP_000522.3:n.78-103_78-102insT
XM_017029556.1:c.78-103_78-102insT	XP_016885045.1:n.78-103_78-102insT
NM_000531.6:c.78-103_78-102insT MANE Select	NP_000522.3:n.78-103_78-102insT