Canonical Allele Identifier: CA402985079
Gene: NDUFS7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1391002G>C , CM000681.2:g.1391002G>C GRCh38
NC_000019.9:g.1391001G>C , CM000681.1:g.1391001G>C GRCh37
NC_000019.8:g.1342001G>C NCBI36
NG_008283.1:g.12119G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233627.14:c.360G>C MANE Select ENSP00000233627.9:p.Met120Ile
ENST00000233627.13:c.360G>C ENSP00000233627.9:p.Met120Ile
ENST00000313408.11:c.360G>C ENSP00000364262.5:p.Met120Ile
ENST00000414651.3:c.450G>C ENSP00000406630.2:p.Met150Ile
ENST00000436115.6:n.2315G>C
ENST00000534853.5:c.*154G>C ENSP00000442822.1:n.*154G>C
ENST00000535382.1:n.612G>C
ENST00000538523.5:n.416G>C
ENST00000538662.5:n.387G>C
ENST00000538929.5:n.450G>C
ENST00000539480.5:c.360G>C ENSP00000443273.1:p.Met120Ile
ENST00000540530.5:n.351G>C
ENST00000543289.5:n.850G>C
ENST00000545446.5:n.651G>C
ENST00000546172.7:c.*356G>C ENSP00000467094.1:n.*356G>C
ENST00000546283.5:c.360G>C ENSP00000440348.1:p.Met120Ile
ENST00000618074.4:c.360G>C ENSP00000477895.1:p.Met120Ile
ENST00000620479.4:c.360G>C ENSP00000480984.1:p.Met120Ile
ENST00000622587.4:n.356G>C
NM_024407.4:c.360G>C NP_077718.3:p.Met120Ile
XM_005259556.3:c.360G>C XP_005259613.2:p.Met120Ile
NM_001363602.1:c.360G>C NP_001350531.1:p.Met120Ile
XM_024451499.1:c.381G>C XP_024307267.1:p.Met127Ile
NM_024407.5:c.360G>C MANE Select NP_077718.3:p.Met120Ile
NM_001363602.2:c.360G>C NP_001350531.1:p.Met120Ile