Canonical Allele Identifier: CA2527249823

Gene: NDUFS7

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1389924_1389925del , CM000681.2:g.1389924_1389925del	GRCh38
NC_000019.9:g.1389923_1389924del , CM000681.1:g.1389923_1389924del	GRCh37
NC_000019.8:g.1340923_1340924del	NCBI36
NG_008283.1:g.11041_11042del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.229-947_229-946del MANE Select	ENSP00000233627.9:n.229-947_229-946del
ENST00000233627.13:c.229-947_229-946del	ENSP00000233627.9:n.229-947_229-946del
ENST00000313408.11:c.229-947_229-946del	ENSP00000364262.5:n.229-947_229-946del
ENST00000414651.3:c.319-947_319-946del	ENSP00000406630.2:n.319-947_319-946del
ENST00000436115.6:n.1237_1238del
ENST00000534853.5:c.*23-947_*23-946del	ENSP00000442822.1:n.*23-947_*23-946del
ENST00000535382.1:n.481-947_481-946del
ENST00000538523.5:n.285-947_285-946del
ENST00000538662.5:n.256-947_256-946del
ENST00000538929.5:n.319-947_319-946del
ENST00000539480.5:c.229-947_229-946del	ENSP00000443273.1:n.229-947_229-946del
ENST00000540530.5:n.220-947_220-946del
ENST00000543289.5:n.719-947_719-946del
ENST00000545446.5:n.520-947_520-946del
ENST00000546172.7:c.*225-947_*225-946del	ENSP00000467094.1:n.*225-947_*225-946del
ENST00000546283.5:c.229-947_229-946del	ENSP00000440348.1:n.229-947_229-946del
ENST00000618074.4:c.229-947_229-946del	ENSP00000477895.1:n.229-947_229-946del
ENST00000620479.4:c.229-947_229-946del	ENSP00000480984.1:n.229-947_229-946del
ENST00000622587.4:n.225-947_225-946del
NM_024407.4:c.229-947_229-946del	NP_077718.3:n.229-947_229-946del
XM_005259556.3:c.229-947_229-946del	XP_005259613.2:n.229-947_229-946del
NM_001363602.1:c.229-947_229-946del	NP_001350531.1:n.229-947_229-946del
XM_024451499.1:c.250-947_250-946del	XP_024307267.1:n.250-947_250-946del
NM_024407.5:c.229-947_229-946del MANE Select	NP_077718.3:n.229-947_229-946del
NM_001363602.2:c.229-947_229-946del	NP_001350531.1:n.229-947_229-946del