Canonical Allele Identifier: CA1674710971

Gene: NOX3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155427880_155427881delinsCT , CM000668.2:g.155427880_155427881delinsCT	GRCh38
NC_000006.11:g.155749014_155749015delinsCT , CM000668.1:g.155749014_155749015delinsCT	GRCh37
NC_000006.10:g.155790706_155790707delinsCT	NCBI36
NG_011995.1:g.33023_33024delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000159060.3:c.1145+913_1145+914delinsAG MANE Select	ENSP00000159060.2:n.1145+913_1145+914delinsAG
ENST00000159060.2:c.1145+913_1145+914delinsAG	ENSP00000159060.2:n.1145+913_1145+914delinsAG
NM_015718.2:c.1145+913_1145+914delinsAG	NP_056533.1:n.1145+913_1145+914delinsAG
NM_015718.3:c.1145+913_1145+914delinsAG MANE Select	NP_056533.1:n.1145+913_1145+914delinsAG