Canonical Allele Identifier: CA2317694904

Gene: NDUFS7

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1391135C= , CM000681.2:g.1391135C=	GRCh38
NC_000019.9:g.1391134C= , CM000681.1:g.1391134C=	GRCh37
NC_000019.8:g.1342134C=	NCBI36
NG_008283.1:g.12252C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.425C= MANE Select	ENSP00000233627.9:p.Pro142=
ENST00000233627.13:c.425C=	ENSP00000233627.9:p.Pro142=
ENST00000313408.11:c.425C=	ENSP00000364262.5:p.Pro142=
ENST00000414651.3:c.515C=	ENSP00000406630.2:p.Pro172=
ENST00000436115.6:n.2380C=
ENST00000534853.5:c.*219C=	ENSP00000442822.1:n.*219C=
ENST00000535382.1:n.677C=
ENST00000538523.5:n.481C=
ENST00000538662.5:n.520C=
ENST00000538929.5:n.515C=
ENST00000539480.5:c.425C=	ENSP00000443273.1:p.Pro142=
ENST00000540530.5:n.416C=
ENST00000543289.5:n.983C=
ENST00000545446.5:n.716C=
ENST00000546172.7:c.*421C=	ENSP00000467094.1:n.*421C=
ENST00000546283.5:c.425C=	ENSP00000440348.1:p.Pro142=
ENST00000618074.4:c.432C=	ENSP00000477895.1:p.Ala144=
ENST00000620479.4:c.429C=	ENSP00000480984.1:p.Ala143=
ENST00000622587.4:n.489C=
NM_024407.4:c.425C=	NP_077718.3:p.Pro142=
XM_005259556.3:c.425C=	XP_005259613.2:p.Pro142=
NM_001363602.1:c.425C=	NP_001350531.1:p.Pro142=
XM_024451499.1:c.446C=	XP_024307267.1:p.Pro149=
NM_024407.5:c.425C= MANE Select	NP_077718.3:p.Pro142=
NM_001363602.2:c.425C=	NP_001350531.1:p.Pro142=