Canonical Allele Identifier: CA1546666202
Gene: NDUFS4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53658412_53658413delinsTA , CM000667.2:g.53658412_53658413delinsTA GRCh38
NC_000005.9:g.52954242_52954243delinsTA , CM000667.1:g.52954242_52954243delinsTA GRCh37
NC_000005.8:g.52989999_52990000delinsTA NCBI36
NG_008200.1:g.102778_102779delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.351-139_351-138delinsTA MANE Select ENSP00000296684.5:n.351-139_351-138delinsTA
ENST00000296684.9:c.351-139_351-138delinsTA ENSP00000296684.5:n.351-139_351-138delinsTA
ENST00000502423.5:c.*218-139_*218-138delinsTA ENSP00000422177.1:n.*218-139_*218-138delinsTA
ENST00000506765.1:c.338+12007_338+12008delinsTA ENSP00000424570.1:n.338+12007_338+12008delinsTA
ENST00000506974.5:c.*127-139_*127-138delinsTA ENSP00000425967.1:n.*127-139_*127-138delinsTA
ENST00000507026.5:c.*325-139_*325-138delinsTA ENSP00000424993.1:n.*325-139_*325-138delinsTA
ENST00000509443.1:n.212-139_212-138delinsTA
NM_002495.2:c.351-139_351-138delinsTA NP_002486.1:n.351-139_351-138delinsTA
XM_005248525.3:c.350+12007_350+12008delinsTA XP_005248582.1:n.350+12007_350+12008delinsTA
XM_011543415.1:c.177-139_177-138delinsTA XP_011541717.1:n.177-139_177-138delinsTA
NM_001318051.1:c.350+12007_350+12008delinsTA NP_001304980.1:n.350+12007_350+12008delinsTA
NM_002495.3:c.351-139_351-138delinsTA NP_002486.1:n.351-139_351-138delinsTA
NR_134473.1:n.553-139_553-138delinsTA
NR_134474.1:n.470-139_470-138delinsTA
NR_134475.1:n.505-139_505-138delinsTA
NM_002495.4:c.351-139_351-138delinsTA MANE Select NP_002486.1:n.351-139_351-138delinsTA
NM_001318051.2:c.350+12007_350+12008delinsTA NP_001304980.1:n.350+12007_350+12008delinsTA
NR_134473.2:n.547-139_547-138delinsTA
NR_134474.2:n.464-139_464-138delinsTA
NR_134475.2:n.499-139_499-138delinsTA