Canonical Allele Identifier: CA2709016564
Gene: NDUFS4 HGNC NCBI

Linked Data

dbSNP Id: rs2112398070

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53560762_53560763insCGTTGAGGACTTCCACATGGAGATTGGCACAGG , CM000667.2:g.53560762_53560763insCGTTGAGGACTTCCACATGGAGATTGGCACAGG GRCh38
NC_000005.9:g.52856592_52856593insCGTTGAGGACTTCCACATGGAGATTGGCACAGG , CM000667.1:g.52856592_52856593insCGTTGAGGACTTCCACATGGAGATTGGCACAGG GRCh37
NC_000005.8:g.52892349_52892350insCGTTGAGGACTTCCACATGGAGATTGGCACAGG NCBI36
NG_008200.1:g.5128_5129insCGTTGAGGACTTCCACATGGAGATTGGCACAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG MANE Select ENSP00000296684.5:n.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCA...
ENST00000296684.9:c.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG ENSP00000296684.5:n.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCA...
ENST00000502423.5:c.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG ENSP00000422177.1:n.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCA...
ENST00000506765.1:c.86+2_86+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG ENSP00000424570.1:n.86+2_86+3insCGTTGAGGACTTCCACATGGAGATTGGCA...
ENST00000506974.5:c.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG ENSP00000425967.1:n.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCA...
ENST00000507026.5:c.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG ENSP00000424993.1:n.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCA...
NM_002495.2:c.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG NP_002486.1:n.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG
XM_005248525.3:c.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG XP_005248582.1:n.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAG...
XM_011543414.1:c.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG XP_011541716.1:n.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAG...
NM_001318051.1:c.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG NP_001304980.1:n.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAG...
NM_002495.3:c.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG NP_002486.1:n.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG
NR_134473.1:n.128+2_128+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG
NR_134474.1:n.128+2_128+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG
NR_134475.1:n.128+2_128+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG
XM_017009491.1:c.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG XP_016864980.1:n.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAG...
NM_002495.4:c.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG MANE Select NP_002486.1:n.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG
NM_001318051.2:c.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG NP_001304980.1:n.98+2_98+3insCGTTGAGGACTTCCACATGGAGATTGGCACAG...
NR_134473.2:n.122+2_122+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG
NR_134474.2:n.122+2_122+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG
NR_134475.2:n.122+2_122+3insCGTTGAGGACTTCCACATGGAGATTGGCACAGG