Canonical Allele Identifier: CA402985176
Gene: NDUFS7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1391015A>G , CM000681.2:g.1391015A>G GRCh38
NC_000019.9:g.1391014A>G , CM000681.1:g.1391014A>G GRCh37
NC_000019.8:g.1342014A>G NCBI36
NG_008283.1:g.12132A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233627.14:c.373A>G MANE Select ENSP00000233627.9:p.Thr125Ala
ENST00000233627.13:c.373A>G ENSP00000233627.9:p.Thr125Ala
ENST00000313408.11:c.373A>G ENSP00000364262.5:p.Thr125Ala
ENST00000414651.3:c.463A>G ENSP00000406630.2:p.Thr155Ala
ENST00000436115.6:n.2328A>G
ENST00000534853.5:c.*167A>G ENSP00000442822.1:n.*167A>G
ENST00000535382.1:n.625A>G
ENST00000538523.5:n.429A>G
ENST00000538662.5:n.400A>G
ENST00000538929.5:n.463A>G
ENST00000539480.5:c.373A>G ENSP00000443273.1:p.Thr125Ala
ENST00000540530.5:n.364A>G
ENST00000543289.5:n.863A>G
ENST00000545446.5:n.664A>G
ENST00000546172.7:c.*369A>G ENSP00000467094.1:n.*369A>G
ENST00000546283.5:c.373A>G ENSP00000440348.1:p.Thr125Ala
ENST00000618074.4:c.373A>G ENSP00000477895.1:p.Thr125Ala
ENST00000620479.4:c.373A>G ENSP00000480984.1:p.Thr125Ala
ENST00000622587.4:n.369A>G
NM_024407.4:c.373A>G NP_077718.3:p.Thr125Ala
XM_005259556.3:c.373A>G XP_005259613.2:p.Thr125Ala
NM_001363602.1:c.373A>G NP_001350531.1:p.Thr125Ala
XM_024451499.1:c.394A>G XP_024307267.1:p.Thr132Ala
NM_024407.5:c.373A>G MANE Select NP_077718.3:p.Thr125Ala
NM_001363602.2:c.373A>G NP_001350531.1:p.Thr125Ala