Canonical Allele Identifier: CA1969462263
Gene: NDUFS3 HGNC NCBI

Linked Data

dbSNP Id: rs2097269295

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582626_47582627del , CM000673.2:g.47582626_47582627del GRCh38
NC_000011.9:g.47604178_47604179del , CM000673.1:g.47604178_47604179del GRCh37
NC_000011.8:g.47560754_47560755del NCBI36
NG_011946.1:g.8617_8618del
NG_011946.2:g.8617_8618del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.627+158_627+159del MANE Select ENSP00000263774.4:n.627+158_627+159del
ENST00000531351.2:n.1822+158_1822+159del
ENST00000677462.1:n.3101+158_3101+159del
ENST00000678975.1:n.2884+158_2884+159del
ENST00000263774.8:c.627+158_627+159del ENSP00000263774.4:n.627+158_627+159del
ENST00000525212.1:n.282+158_282+159del
ENST00000525378.5:n.565+158_565+159del
ENST00000527178.1:n.227+158_227+159del
ENST00000533507.5:n.1521+158_1521+159del
NM_004551.2:c.627+158_627+159del NP_004542.1:n.627+158_627+159del
NM_004551.3:c.627+158_627+159del MANE Select NP_004542.1:n.627+158_627+159del