Canonical Allele Identifier: CA2582636100
Gene: NDUFS7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1389065_1389090del , CM000681.2:g.1389065_1389090del GRCh38
NC_000019.9:g.1389064_1389089del , CM000681.1:g.1389064_1389089del GRCh37
NC_000019.8:g.1340064_1340089del NCBI36
NG_008283.1:g.10182_10207del

Transcript Alleles

HGVS Amino-acid change
ENST00000233627.14:c.228+127_228+152del MANE Select ENSP00000233627.9:n.228+127_228+152del
ENST00000233627.13:c.228+127_228+152del ENSP00000233627.9:n.228+127_228+152del
ENST00000313408.11:c.228+127_228+152del ENSP00000364262.5:n.228+127_228+152del
ENST00000414651.3:c.318+127_318+152del ENSP00000406630.2:n.318+127_318+152del
ENST00000436115.6:n.378_403del
ENST00000534853.5:c.*22+127_*22+152del ENSP00000442822.1:n.*22+127_*22+152del
ENST00000535382.1:n.480+127_480+152del
ENST00000538523.5:n.284+127_284+152del
ENST00000538662.5:n.255+127_255+152del
ENST00000538929.5:n.318+127_318+152del
ENST00000539480.5:c.228+127_228+152del ENSP00000443273.1:n.228+127_228+152del
ENST00000540530.5:n.219+127_219+152del
ENST00000543289.5:n.718+127_718+152del
ENST00000545446.5:n.519+127_519+152del
ENST00000546172.7:c.*224+127_*224+152del ENSP00000467094.1:n.*224+127_*224+152del
ENST00000546283.5:c.228+127_228+152del ENSP00000440348.1:n.228+127_228+152del
ENST00000618074.4:c.228+127_228+152del ENSP00000477895.1:n.228+127_228+152del
ENST00000620479.4:c.228+127_228+152del ENSP00000480984.1:n.228+127_228+152del
ENST00000622587.4:n.224+127_224+152del
NM_024407.4:c.228+127_228+152del NP_077718.3:n.228+127_228+152del
XM_005259556.3:c.228+127_228+152del XP_005259613.2:n.228+127_228+152del
NM_001363602.1:c.228+127_228+152del NP_001350531.1:n.228+127_228+152del
XM_017026768.2:c.355_380del XP_016882257.2:p.Ala119MetfsTer?
XM_024451499.1:c.249+127_249+152del XP_024307267.1:n.249+127_249+152del
NM_024407.5:c.228+127_228+152del MANE Select NP_077718.3:n.228+127_228+152del
NM_001363602.2:c.228+127_228+152del NP_001350531.1:n.228+127_228+152del