Canonical Allele Identifier: CA783452086
Gene: NDUFS7 HGNC NCBI

Linked Data

dbSNP Id: rs1441390444

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1391506_1391507del , CM000681.2:g.1391506_1391507del GRCh38
NC_000019.9:g.1391505_1391506del , CM000681.1:g.1391505_1391506del GRCh37
NC_000019.8:g.1342505_1342506del NCBI36
NG_008283.1:g.12623_12624del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233627.14:c.455+341_455+342del MANE Select ENSP00000233627.9:n.455+341_455+342del
ENST00000233627.13:c.455+341_455+342del ENSP00000233627.9:n.455+341_455+342del
ENST00000313408.11:c.455+341_455+342del ENSP00000364262.5:n.455+341_455+342del
ENST00000414651.3:c.545+341_545+342del ENSP00000406630.2:n.545+341_545+342del
ENST00000436115.6:n.2410+341_2410+342del
ENST00000534853.5:c.*249+341_*249+342del ENSP00000442822.1:n.*249+341_*249+342del
ENST00000535382.1:n.707+341_707+342del
ENST00000538523.5:n.511+341_511+342del
ENST00000538662.5:n.550+341_550+342del
ENST00000538929.5:n.545+341_545+342del
ENST00000539480.5:c.455+341_455+342del ENSP00000443273.1:n.455+341_455+342del
ENST00000540530.5:n.446+341_446+342del
ENST00000543289.5:n.1013+341_1013+342del
ENST00000545446.5:n.746+341_746+342del
ENST00000546172.7:c.*451+341_*451+342del ENSP00000467094.1:n.*451+341_*451+342del
ENST00000546283.5:c.455+341_455+342del ENSP00000440348.1:n.455+341_455+342del
ENST00000618074.4:c.462+341_462+342del ENSP00000477895.1:n.462+341_462+342del
ENST00000620479.4:c.459+341_459+342del ENSP00000480984.1:n.459+341_459+342del
ENST00000622587.4:n.519+341_519+342del
NM_024407.4:c.455+341_455+342del NP_077718.3:n.455+341_455+342del
XM_005259556.3:c.455+341_455+342del XP_005259613.2:n.455+341_455+342del
NM_001363602.1:c.455+341_455+342del NP_001350531.1:n.455+341_455+342del
XM_024451499.1:c.476+341_476+342del XP_024307267.1:n.476+341_476+342del
NM_024407.5:c.455+341_455+342del MANE Select NP_077718.3:n.455+341_455+342del
NM_001363602.2:c.455+341_455+342del NP_001350531.1:n.455+341_455+342del