Canonical Allele Identifier: CA2582636208
Gene: NDUFS7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1389165_1389166dup , CM000681.2:g.1389165_1389166dup GRCh38
NC_000019.9:g.1389164_1389165dup , CM000681.1:g.1389164_1389165dup GRCh37
NC_000019.8:g.1340164_1340165dup NCBI36
NG_008283.1:g.10282_10283dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000233627.14:c.228+227_228+228dup MANE Select ENSP00000233627.9:n.228+227_228+228dup
ENST00000233627.13:c.228+227_228+228dup ENSP00000233627.9:n.228+227_228+228dup
ENST00000313408.11:c.228+227_228+228dup ENSP00000364262.5:n.228+227_228+228dup
ENST00000414651.3:c.318+227_318+228dup ENSP00000406630.2:n.318+227_318+228dup
ENST00000436115.6:n.478_479dup
ENST00000534853.5:c.*22+227_*22+228dup ENSP00000442822.1:n.*22+227_*22+228dup
ENST00000535382.1:n.480+227_480+228dup
ENST00000538523.5:n.284+227_284+228dup
ENST00000538662.5:n.255+227_255+228dup
ENST00000538929.5:n.318+227_318+228dup
ENST00000539480.5:c.228+227_228+228dup ENSP00000443273.1:n.228+227_228+228dup
ENST00000540530.5:n.219+227_219+228dup
ENST00000543289.5:n.718+227_718+228dup
ENST00000545446.5:n.519+227_519+228dup
ENST00000546172.7:c.*224+227_*224+228dup ENSP00000467094.1:n.*224+227_*224+228dup
ENST00000546283.5:c.228+227_228+228dup ENSP00000440348.1:n.228+227_228+228dup
ENST00000618074.4:c.228+227_228+228dup ENSP00000477895.1:n.228+227_228+228dup
ENST00000620479.4:c.228+227_228+228dup ENSP00000480984.1:n.228+227_228+228dup
ENST00000622587.4:n.224+227_224+228dup
NM_024407.4:c.228+227_228+228dup NP_077718.3:n.228+227_228+228dup
XM_005259556.3:c.228+227_228+228dup XP_005259613.2:n.228+227_228+228dup
NM_001363602.1:c.228+227_228+228dup NP_001350531.1:n.228+227_228+228dup
XM_017026768.2:c.455_456dup XP_016882257.2:p.Leu153ThrfsTer?
XM_024451499.1:c.249+227_249+228dup XP_024307267.1:n.249+227_249+228dup
NM_024407.5:c.228+227_228+228dup MANE Select NP_077718.3:n.228+227_228+228dup
NM_001363602.2:c.228+227_228+228dup NP_001350531.1:n.228+227_228+228dup