Canonical Allele Identifier: CA992511927
Gene: NDUFS7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1391504_1391514del , CM000681.2:g.1391504_1391514del GRCh38
NC_000019.9:g.1391503_1391513del , CM000681.1:g.1391503_1391513del GRCh37
NC_000019.8:g.1342503_1342513del NCBI36
NG_008283.1:g.12621_12631del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233627.14:c.455+339_455+349del MANE Select ENSP00000233627.9:n.455+339_455+349del
ENST00000233627.13:c.455+339_455+349del ENSP00000233627.9:n.455+339_455+349del
ENST00000313408.11:c.455+339_455+349del ENSP00000364262.5:n.455+339_455+349del
ENST00000414651.3:c.545+339_545+349del ENSP00000406630.2:n.545+339_545+349del
ENST00000436115.6:n.2410+339_2410+349del
ENST00000534853.5:c.*249+339_*249+349del ENSP00000442822.1:n.*249+339_*249+349del
ENST00000535382.1:n.707+339_707+349del
ENST00000538523.5:n.511+339_511+349del
ENST00000538662.5:n.550+339_550+349del
ENST00000538929.5:n.545+339_545+349del
ENST00000539480.5:c.455+339_455+349del ENSP00000443273.1:n.455+339_455+349del
ENST00000540530.5:n.446+339_446+349del
ENST00000543289.5:n.1013+339_1013+349del
ENST00000545446.5:n.746+339_746+349del
ENST00000546172.7:c.*451+339_*451+349del ENSP00000467094.1:n.*451+339_*451+349del
ENST00000546283.5:c.455+339_455+349del ENSP00000440348.1:n.455+339_455+349del
ENST00000618074.4:c.462+339_462+349del ENSP00000477895.1:n.462+339_462+349del
ENST00000620479.4:c.459+339_459+349del ENSP00000480984.1:n.459+339_459+349del
ENST00000622587.4:n.519+339_519+349del
NM_024407.4:c.455+339_455+349del NP_077718.3:n.455+339_455+349del
XM_005259556.3:c.455+339_455+349del XP_005259613.2:n.455+339_455+349del
NM_001363602.1:c.455+339_455+349del NP_001350531.1:n.455+339_455+349del
XM_024451499.1:c.476+339_476+349del XP_024307267.1:n.476+339_476+349del
NM_024407.5:c.455+339_455+349del MANE Select NP_077718.3:n.455+339_455+349del
NM_001363602.2:c.455+339_455+349del NP_001350531.1:n.455+339_455+349del