Canonical Allele Identifier: CA2317694191
Gene: NDUFS7 HGNC NCBI

Linked Data

dbSNP Id: rs1805048258

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1389912_1389913insGT , CM000681.2:g.1389912_1389913insGT GRCh38
NC_000019.9:g.1389911_1389912insGT , CM000681.1:g.1389911_1389912insGT GRCh37
NC_000019.8:g.1340911_1340912insGT NCBI36
NG_008283.1:g.11029_11030insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000233627.14:c.229-959_229-958insGT MANE Select ENSP00000233627.9:n.229-959_229-958insGT
ENST00000233627.13:c.229-959_229-958insGT ENSP00000233627.9:n.229-959_229-958insGT
ENST00000313408.11:c.229-959_229-958insGT ENSP00000364262.5:n.229-959_229-958insGT
ENST00000414651.3:c.319-959_319-958insGT ENSP00000406630.2:n.319-959_319-958insGT
ENST00000436115.6:n.1225_1226insGT
ENST00000534853.5:c.*23-959_*23-958insGT ENSP00000442822.1:n.*23-959_*23-958insGT
ENST00000535382.1:n.481-959_481-958insGT
ENST00000538523.5:n.285-959_285-958insGT
ENST00000538662.5:n.256-959_256-958insGT
ENST00000538929.5:n.319-959_319-958insGT
ENST00000539480.5:c.229-959_229-958insGT ENSP00000443273.1:n.229-959_229-958insGT
ENST00000540530.5:n.220-959_220-958insGT
ENST00000543289.5:n.719-959_719-958insGT
ENST00000545446.5:n.520-959_520-958insGT
ENST00000546172.7:c.*225-959_*225-958insGT ENSP00000467094.1:n.*225-959_*225-958insGT
ENST00000546283.5:c.229-959_229-958insGT ENSP00000440348.1:n.229-959_229-958insGT
ENST00000618074.4:c.229-959_229-958insGT ENSP00000477895.1:n.229-959_229-958insGT
ENST00000620479.4:c.229-959_229-958insGT ENSP00000480984.1:n.229-959_229-958insGT
ENST00000622587.4:n.225-959_225-958insGT
NM_024407.4:c.229-959_229-958insGT NP_077718.3:n.229-959_229-958insGT
XM_005259556.3:c.229-959_229-958insGT XP_005259613.2:n.229-959_229-958insGT
NM_001363602.1:c.229-959_229-958insGT NP_001350531.1:n.229-959_229-958insGT
XM_024451499.1:c.250-959_250-958insGT XP_024307267.1:n.250-959_250-958insGT
NM_024407.5:c.229-959_229-958insGT MANE Select NP_077718.3:n.229-959_229-958insGT
NM_001363602.2:c.229-959_229-958insGT NP_001350531.1:n.229-959_229-958insGT