Canonical Allele Identifier: CA2813255804

Gene: NDUFS7

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1389912_1389913insG , CM000681.2:g.1389912_1389913insG	GRCh38
NC_000019.9:g.1389911_1389912insG , CM000681.1:g.1389911_1389912insG	GRCh37
NC_000019.8:g.1340911_1340912insG	NCBI36
NG_008283.1:g.11029_11030insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.229-959_229-958insG MANE Select	ENSP00000233627.9:n.229-959_229-958insG
ENST00000233627.13:c.229-959_229-958insG	ENSP00000233627.9:n.229-959_229-958insG
ENST00000313408.11:c.229-959_229-958insG	ENSP00000364262.5:n.229-959_229-958insG
ENST00000414651.3:c.319-959_319-958insG	ENSP00000406630.2:n.319-959_319-958insG
ENST00000436115.6:n.1225_1226insG
ENST00000534853.5:c.*23-959_*23-958insG	ENSP00000442822.1:n.*23-959_*23-958insG
ENST00000535382.1:n.481-959_481-958insG
ENST00000538523.5:n.285-959_285-958insG
ENST00000538662.5:n.256-959_256-958insG
ENST00000538929.5:n.319-959_319-958insG
ENST00000539480.5:c.229-959_229-958insG	ENSP00000443273.1:n.229-959_229-958insG
ENST00000540530.5:n.220-959_220-958insG
ENST00000543289.5:n.719-959_719-958insG
ENST00000545446.5:n.520-959_520-958insG
ENST00000546172.7:c.*225-959_*225-958insG	ENSP00000467094.1:n.*225-959_*225-958insG
ENST00000546283.5:c.229-959_229-958insG	ENSP00000440348.1:n.229-959_229-958insG
ENST00000618074.4:c.229-959_229-958insG	ENSP00000477895.1:n.229-959_229-958insG
ENST00000620479.4:c.229-959_229-958insG	ENSP00000480984.1:n.229-959_229-958insG
ENST00000622587.4:n.225-959_225-958insG
NM_024407.4:c.229-959_229-958insG	NP_077718.3:n.229-959_229-958insG
XM_005259556.3:c.229-959_229-958insG	XP_005259613.2:n.229-959_229-958insG
NM_001363602.1:c.229-959_229-958insG	NP_001350531.1:n.229-959_229-958insG
XM_024451499.1:c.250-959_250-958insG	XP_024307267.1:n.250-959_250-958insG
NM_024407.5:c.229-959_229-958insG MANE Select	NP_077718.3:n.229-959_229-958insG
NM_001363602.2:c.229-959_229-958insG	NP_001350531.1:n.229-959_229-958insG