Canonical Allele Identifier: CA2582636765
Gene: NDUFS7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1389912_1389937del , CM000681.2:g.1389912_1389937del GRCh38
NC_000019.9:g.1389911_1389936del , CM000681.1:g.1389911_1389936del GRCh37
NC_000019.8:g.1340911_1340936del NCBI36
NG_008283.1:g.11029_11054del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233627.14:c.229-959_229-934del MANE Select ENSP00000233627.9:n.229-959_229-934del
ENST00000233627.13:c.229-959_229-934del ENSP00000233627.9:n.229-959_229-934del
ENST00000313408.11:c.229-959_229-934del ENSP00000364262.5:n.229-959_229-934del
ENST00000414651.3:c.319-959_319-934del ENSP00000406630.2:n.319-959_319-934del
ENST00000436115.6:n.1225_1250del
ENST00000534853.5:c.*23-959_*23-934del ENSP00000442822.1:n.*23-959_*23-934del
ENST00000535382.1:n.481-959_481-934del
ENST00000538523.5:n.285-959_285-934del
ENST00000538662.5:n.256-959_256-934del
ENST00000538929.5:n.319-959_319-934del
ENST00000539480.5:c.229-959_229-934del ENSP00000443273.1:n.229-959_229-934del
ENST00000540530.5:n.220-959_220-934del
ENST00000543289.5:n.719-959_719-934del
ENST00000545446.5:n.520-959_520-934del
ENST00000546172.7:c.*225-959_*225-934del ENSP00000467094.1:n.*225-959_*225-934del
ENST00000546283.5:c.229-959_229-934del ENSP00000440348.1:n.229-959_229-934del
ENST00000618074.4:c.229-959_229-934del ENSP00000477895.1:n.229-959_229-934del
ENST00000620479.4:c.229-959_229-934del ENSP00000480984.1:n.229-959_229-934del
ENST00000622587.4:n.225-959_225-934del
NM_024407.4:c.229-959_229-934del NP_077718.3:n.229-959_229-934del
XM_005259556.3:c.229-959_229-934del XP_005259613.2:n.229-959_229-934del
NM_001363602.1:c.229-959_229-934del NP_001350531.1:n.229-959_229-934del
XM_024451499.1:c.250-959_250-934del XP_024307267.1:n.250-959_250-934del
NM_024407.5:c.229-959_229-934del MANE Select NP_077718.3:n.229-959_229-934del
NM_001363602.2:c.229-959_229-934del NP_001350531.1:n.229-959_229-934del