Canonical Allele Identifier: CA2535930644

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38367138_38367139insGGGG , CM000685.2:g.38367138_38367139insGGGG	GRCh38
NC_000023.10:g.38226391_38226392insGGGG , CM000685.1:g.38226391_38226392insGGGG	GRCh37
NC_000023.9:g.38111335_38111336insGGGG	NCBI36
NG_008471.1:g.19656_19657insGGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000039007.5:c.78-153_78-152insGGGG MANE Select	ENSP00000039007.4:n.78-153_78-152insGGGG
ENST00000643344.1:c.78-153_78-152insGGGG	ENSP00000496606.1:n.78-153_78-152insGGGG
ENST00000039007.4:c.78-153_78-152insGGGG	ENSP00000039007.4:n.78-153_78-152insGGGG
ENST00000465127.1:c.172-298983_172-298982insGGGG	ENSP00000417050.1:n.172-298983_172-298982...
ENST00000488812.1:n.170-153_170-152insGGGG
NM_000531.5:c.78-153_78-152insGGGG	NP_000522.3:n.78-153_78-152insGGGG
XM_017029556.1:c.78-153_78-152insGGGG	XP_016885045.1:n.78-153_78-152insGGGG
NM_000531.6:c.78-153_78-152insGGGG MANE Select	NP_000522.3:n.78-153_78-152insGGGG