Canonical Allele Identifier: CA2317695103

Gene: NDUFS7

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1391479_1391486delinsTTTTTTTC , CM000681.2:g.1391479_1391486delinsTTTTTTTC	GRCh38
NC_000019.9:g.1391478_1391485delinsTTTTTTTC , CM000681.1:g.1391478_1391485delinsTTTTTTTC	GRCh37
NC_000019.8:g.1342478_1342485delinsTTTTTTTC	NCBI36
NG_008283.1:g.12596_12603delinsTTTTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.455+314_455+321delinsTTTTTTTC MANE Select	ENSP00000233627.9:n.455+314_455+321delinsTTTTTTTC
ENST00000233627.13:c.455+314_455+321delinsTTTTTTTC	ENSP00000233627.9:n.455+314_455+321delinsTTTTTTTC
ENST00000313408.11:c.455+314_455+321delinsTTTTTTTC	ENSP00000364262.5:n.455+314_455+321delinsTTTTTTTC
ENST00000414651.3:c.545+314_545+321delinsTTTTTTTC	ENSP00000406630.2:n.545+314_545+321delinsTTTTTTTC
ENST00000436115.6:n.2410+314_2410+321delinsTTTTTTTC
ENST00000534853.5:c.*249+314_*249+321delinsTTTTTTTC	ENSP00000442822.1:n.*249+314_*249+321delinsTTTTTTTC
ENST00000535382.1:n.707+314_707+321delinsTTTTTTTC
ENST00000538523.5:n.511+314_511+321delinsTTTTTTTC
ENST00000538662.5:n.550+314_550+321delinsTTTTTTTC
ENST00000538929.5:n.545+314_545+321delinsTTTTTTTC
ENST00000539480.5:c.455+314_455+321delinsTTTTTTTC	ENSP00000443273.1:n.455+314_455+321delinsTTTTTTTC
ENST00000540530.5:n.446+314_446+321delinsTTTTTTTC
ENST00000543289.5:n.1013+314_1013+321delinsTTTTTTTC
ENST00000545446.5:n.746+314_746+321delinsTTTTTTTC
ENST00000546172.7:c.*451+314_*451+321delinsTTTTTTTC	ENSP00000467094.1:n.*451+314_*451+321delinsTTTTTTTC
ENST00000546283.5:c.455+314_455+321delinsTTTTTTTC	ENSP00000440348.1:n.455+314_455+321delinsTTTTTTTC
ENST00000618074.4:c.462+314_462+321delinsTTTTTTTC	ENSP00000477895.1:n.462+314_462+321delinsTTTTTTTC
ENST00000620479.4:c.459+314_459+321delinsTTTTTTTC	ENSP00000480984.1:n.459+314_459+321delinsTTTTTTTC
ENST00000622587.4:n.519+314_519+321delinsTTTTTTTC
NM_024407.4:c.455+314_455+321delinsTTTTTTTC	NP_077718.3:n.455+314_455+321delinsTTTTTTTC
XM_005259556.3:c.455+314_455+321delinsTTTTTTTC	XP_005259613.2:n.455+314_455+321delinsTTTTTTTC
NM_001363602.1:c.455+314_455+321delinsTTTTTTTC	NP_001350531.1:n.455+314_455+321delinsTTTTTTTC
XM_024451499.1:c.476+314_476+321delinsTTTTTTTC	XP_024307267.1:n.476+314_476+321delinsTTTTTTTC
NM_024407.5:c.455+314_455+321delinsTTTTTTTC MANE Select	NP_077718.3:n.455+314_455+321delinsTTTTTTTC
NM_001363602.2:c.455+314_455+321delinsTTTTTTTC	NP_001350531.1:n.455+314_455+321delinsTTTTTTTC