Canonical Allele Identifier: CA2317695134

Gene: NDUFS7

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1391502_1391504delinsTTG , CM000681.2:g.1391502_1391504delinsTTG	GRCh38
NC_000019.9:g.1391501_1391503delinsTTG , CM000681.1:g.1391501_1391503delinsTTG	GRCh37
NC_000019.8:g.1342501_1342503delinsTTG	NCBI36
NG_008283.1:g.12619_12621delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.455+337_455+339delinsTTG MANE Select	ENSP00000233627.9:n.455+337_455+339delinsTTG
ENST00000233627.13:c.455+337_455+339delinsTTG	ENSP00000233627.9:n.455+337_455+339delinsTTG
ENST00000313408.11:c.455+337_455+339delinsTTG	ENSP00000364262.5:n.455+337_455+339delinsTTG
ENST00000414651.3:c.545+337_545+339delinsTTG	ENSP00000406630.2:n.545+337_545+339delinsTTG
ENST00000436115.6:n.2410+337_2410+339delinsTTG
ENST00000534853.5:c.*249+337_*249+339delinsTTG	ENSP00000442822.1:n.*249+337_*249+339delinsTTG
ENST00000535382.1:n.707+337_707+339delinsTTG
ENST00000538523.5:n.511+337_511+339delinsTTG
ENST00000538662.5:n.550+337_550+339delinsTTG
ENST00000538929.5:n.545+337_545+339delinsTTG
ENST00000539480.5:c.455+337_455+339delinsTTG	ENSP00000443273.1:n.455+337_455+339delinsTTG
ENST00000540530.5:n.446+337_446+339delinsTTG
ENST00000543289.5:n.1013+337_1013+339delinsTTG
ENST00000545446.5:n.746+337_746+339delinsTTG
ENST00000546172.7:c.*451+337_*451+339delinsTTG	ENSP00000467094.1:n.*451+337_*451+339delinsTTG
ENST00000546283.5:c.455+337_455+339delinsTTG	ENSP00000440348.1:n.455+337_455+339delinsTTG
ENST00000618074.4:c.462+337_462+339delinsTTG	ENSP00000477895.1:n.462+337_462+339delinsTTG
ENST00000620479.4:c.459+337_459+339delinsTTG	ENSP00000480984.1:n.459+337_459+339delinsTTG
ENST00000622587.4:n.519+337_519+339delinsTTG
NM_024407.4:c.455+337_455+339delinsTTG	NP_077718.3:n.455+337_455+339delinsTTG
XM_005259556.3:c.455+337_455+339delinsTTG	XP_005259613.2:n.455+337_455+339delinsTTG
NM_001363602.1:c.455+337_455+339delinsTTG	NP_001350531.1:n.455+337_455+339delinsTTG
XM_024451499.1:c.476+337_476+339delinsTTG	XP_024307267.1:n.476+337_476+339delinsTTG
NM_024407.5:c.455+337_455+339delinsTTG MANE Select	NP_077718.3:n.455+337_455+339delinsTTG
NM_001363602.2:c.455+337_455+339delinsTTG	NP_001350531.1:n.455+337_455+339delinsTTG