Canonical Allele Identifier: CA2317694914
Gene: NDUFS7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1391148C= , CM000681.2:g.1391148C= GRCh38
NC_000019.9:g.1391147C= , CM000681.1:g.1391147C= GRCh37
NC_000019.8:g.1342147C= NCBI36
NG_008283.1:g.12265C=

Transcript Alleles

HGVS Amino-acid change
ENST00000233627.14:c.438C= MANE Select ENSP00000233627.9:p.Tyr146=
ENST00000233627.13:c.438C= ENSP00000233627.9:p.Tyr146=
ENST00000313408.11:c.438C= ENSP00000364262.5:p.Tyr146=
ENST00000414651.3:c.528C= ENSP00000406630.2:p.Tyr176=
ENST00000436115.6:n.2393C=
ENST00000534853.5:c.*232C= ENSP00000442822.1:n.*232C=
ENST00000535382.1:n.690C=
ENST00000538523.5:n.494C=
ENST00000538662.5:n.533C=
ENST00000538929.5:n.528C=
ENST00000539480.5:c.438C= ENSP00000443273.1:p.Tyr146=
ENST00000540530.5:n.429C=
ENST00000543289.5:n.996C=
ENST00000545446.5:n.729C=
ENST00000546172.7:c.*434C= ENSP00000467094.1:n.*434C=
ENST00000546283.5:c.438C= ENSP00000440348.1:p.Tyr146=
ENST00000618074.4:c.445C= ENSP00000477895.1:p.Arg149=
ENST00000620479.4:c.442C= ENSP00000480984.1:p.Arg148=
ENST00000622587.4:n.502C=
NM_024407.4:c.438C= NP_077718.3:p.Tyr146=
XM_005259556.3:c.438C= XP_005259613.2:p.Tyr146=
NM_001363602.1:c.438C= NP_001350531.1:p.Tyr146=
XM_024451499.1:c.459C= XP_024307267.1:p.Tyr153=
NM_024407.5:c.438C= MANE Select NP_077718.3:p.Tyr146=
NM_001363602.2:c.438C= NP_001350531.1:p.Tyr146=