Canonical Allele Identifier: CA1969462203
Gene: NDUFS3 HGNC NCBI

Linked Data

dbSNP Id: rs1799506251

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582469_47582470dup , CM000673.2:g.47582469_47582470dup GRCh38
NC_000011.9:g.47604021_47604022dup , CM000673.1:g.47604021_47604022dup GRCh37
NC_000011.8:g.47560597_47560598dup NCBI36
NG_011946.1:g.8460_8461dup
NG_011946.2:g.8460_8461dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.627+1_627+2dup MANE Select ENSP00000263774.4:n.627+1_627+2dup
ENST00000531351.2:n.1822+1_1822+2dup
ENST00000677462.1:n.3101+1_3101+2dup
ENST00000678975.1:n.2884+1_2884+2dup
ENST00000263774.8:c.627+1_627+2dup ENSP00000263774.4:n.627+1_627+2dup
ENST00000524568.1:n.731_732dup
ENST00000525212.1:n.282+1_282+2dup
ENST00000525378.5:n.565+1_565+2dup
ENST00000527178.1:n.227+1_227+2dup
ENST00000533507.5:n.1521+1_1521+2dup
NM_004551.2:c.627+1_627+2dup NP_004542.1:n.627+1_627+2dup
NM_004551.3:c.627+1_627+2dup MANE Select NP_004542.1:n.627+1_627+2dup