Canonical Allele Identifier: CA2317695143

Gene: NDUFS7

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1391508_1391510delinsCAG , CM000681.2:g.1391508_1391510delinsCAG	GRCh38
NC_000019.9:g.1391507_1391509delinsCAG , CM000681.1:g.1391507_1391509delinsCAG	GRCh37
NC_000019.8:g.1342507_1342509delinsCAG	NCBI36
NG_008283.1:g.12625_12627delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.455+343_455+345delinsCAG MANE Select	ENSP00000233627.9:n.455+343_455+345delinsCAG
ENST00000233627.13:c.455+343_455+345delinsCAG	ENSP00000233627.9:n.455+343_455+345delinsCAG
ENST00000313408.11:c.455+343_455+345delinsCAG	ENSP00000364262.5:n.455+343_455+345delinsCAG
ENST00000414651.3:c.545+343_545+345delinsCAG	ENSP00000406630.2:n.545+343_545+345delinsCAG
ENST00000436115.6:n.2410+343_2410+345delinsCAG
ENST00000534853.5:c.*249+343_*249+345delinsCAG	ENSP00000442822.1:n.*249+343_*249+345delinsCAG
ENST00000535382.1:n.707+343_707+345delinsCAG
ENST00000538523.5:n.511+343_511+345delinsCAG
ENST00000538662.5:n.550+343_550+345delinsCAG
ENST00000538929.5:n.545+343_545+345delinsCAG
ENST00000539480.5:c.455+343_455+345delinsCAG	ENSP00000443273.1:n.455+343_455+345delinsCAG
ENST00000540530.5:n.446+343_446+345delinsCAG
ENST00000543289.5:n.1013+343_1013+345delinsCAG
ENST00000545446.5:n.746+343_746+345delinsCAG
ENST00000546172.7:c.*451+343_*451+345delinsCAG	ENSP00000467094.1:n.*451+343_*451+345delinsCAG
ENST00000546283.5:c.455+343_455+345delinsCAG	ENSP00000440348.1:n.455+343_455+345delinsCAG
ENST00000618074.4:c.462+343_462+345delinsCAG	ENSP00000477895.1:n.462+343_462+345delinsCAG
ENST00000620479.4:c.459+343_459+345delinsCAG	ENSP00000480984.1:n.459+343_459+345delinsCAG
ENST00000622587.4:n.519+343_519+345delinsCAG
NM_024407.4:c.455+343_455+345delinsCAG	NP_077718.3:n.455+343_455+345delinsCAG
XM_005259556.3:c.455+343_455+345delinsCAG	XP_005259613.2:n.455+343_455+345delinsCAG
NM_001363602.1:c.455+343_455+345delinsCAG	NP_001350531.1:n.455+343_455+345delinsCAG
XM_024451499.1:c.476+343_476+345delinsCAG	XP_024307267.1:n.476+343_476+345delinsCAG
NM_024407.5:c.455+343_455+345delinsCAG MANE Select	NP_077718.3:n.455+343_455+345delinsCAG
NM_001363602.2:c.455+343_455+345delinsCAG	NP_001350531.1:n.455+343_455+345delinsCAG