Canonical Allele Identifier: CA1320914017

Gene: NDUFB3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201085642_201085643delinsGT , CM000664.2:g.201085642_201085643delinsGT	GRCh38
NC_000002.11:g.201950365_201950366delinsGT , CM000664.1:g.201950365_201950366delinsGT	GRCh37
NC_000002.10:g.201658610_201658611delinsGT	NCBI36
NG_032156.1:g.18904_18905delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682325.1:c.*27_*28delinsGT	ENSP00000507925.1:n.*27_*28delinsGT
ENST00000684175.1:c.*27_*28delinsGT	ENSP00000508132.1:n.*27_*28delinsGT
ENST00000684420.1:c.*27_*28delinsGT	ENSP00000508208.1:n.*27_*28delinsGT
ENST00000237889.9:c.*27_*28delinsGT MANE Select	ENSP00000237889.4:n.*27_*28delinsGT
ENST00000237889.8:c.*27_*28delinsGT	ENSP00000237889.4:n.*27_*28delinsGT
ENST00000433898.5:c.*27_*28delinsGT	ENSP00000410600.1:n.*27_*28delinsGT
ENST00000454214.1:c.*27_*28delinsGT	ENSP00000407336.1:n.*27_*28delinsGT
NM_001257102.1:c.*27_*28delinsGT	NP_001244031.1:n.*27_*28delinsGT
NM_002491.2:c.*27_*28delinsGT	NP_002482.1:n.*27_*28delinsGT
XM_011511230.1:c.*27_*28delinsGT	XP_011509532.1:n.*27_*28delinsGT
XM_011511230.3:c.*27_*28delinsGT	XP_011509532.1:n.*27_*28delinsGT
XM_017004186.2:c.*27_*28delinsGT	XP_016859675.1:n.*27_*28delinsGT
NM_002491.3:c.*27_*28delinsGT MANE Select	NP_002482.1:n.*27_*28delinsGT
NM_001257102.2:c.*27_*28delinsGT	NP_001244031.1:n.*27_*28delinsGT