Canonical Allele Identifier: CA1969462237
Gene: NDUFS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582563_47582566delinsTGTG , CM000673.2:g.47582563_47582566delinsTGTG GRCh38
NC_000011.9:g.47604115_47604118delinsTGTG , CM000673.1:g.47604115_47604118delinsTGTG GRCh37
NC_000011.8:g.47560691_47560694delinsTGTG NCBI36
NG_011946.1:g.8554_8557delinsTGTG
NG_011946.2:g.8554_8557delinsTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.627+95_627+98delinsTGTG MANE Select ENSP00000263774.4:n.627+95_627+98delinsTGTG
ENST00000531351.2:n.1822+95_1822+98delinsTGTG
ENST00000677462.1:n.3101+95_3101+98delinsTGTG
ENST00000678975.1:n.2884+95_2884+98delinsTGTG
ENST00000263774.8:c.627+95_627+98delinsTGTG ENSP00000263774.4:n.627+95_627+98delinsTGTG
ENST00000525212.1:n.282+95_282+98delinsTGTG
ENST00000525378.5:n.565+95_565+98delinsTGTG
ENST00000527178.1:n.227+95_227+98delinsTGTG
ENST00000533507.5:n.1521+95_1521+98delinsTGTG
NM_004551.2:c.627+95_627+98delinsTGTG NP_004542.1:n.627+95_627+98delinsTGTG
NM_004551.3:c.627+95_627+98delinsTGTG MANE Select NP_004542.1:n.627+95_627+98delinsTGTG