Canonical Allele Identifier: CA2514538100

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38367138_38367139insATG , CM000685.2:g.38367138_38367139insATG	GRCh38
NC_000023.10:g.38226391_38226392insATG , CM000685.1:g.38226391_38226392insATG	GRCh37
NC_000023.9:g.38111335_38111336insATG	NCBI36
NG_008471.1:g.19656_19657insATG

Transcript Alleles

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