Canonical Allele Identifier: CA2317693346

Gene: NDUFS7

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1388905C= , CM000681.2:g.1388905C=	GRCh38
NC_000019.9:g.1388904C= , CM000681.1:g.1388904C=	GRCh37
NC_000019.8:g.1339904C=	NCBI36
NG_008283.1:g.10022C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.195C= MANE Select	ENSP00000233627.9:p.Ala65=
ENST00000233627.13:c.195C=	ENSP00000233627.9:p.Ala65=
ENST00000313408.11:c.195C=	ENSP00000364262.5:p.Ala65=
ENST00000414651.3:c.285C=	ENSP00000406630.2:p.Ala95=
ENST00000436115.6:n.218C=
ENST00000534853.5:c.190C=	ENSP00000442822.1:p.Gln64=
ENST00000535382.1:n.447C=
ENST00000538523.5:n.251C=
ENST00000538662.5:n.222C=
ENST00000538929.5:n.285C=
ENST00000539480.5:c.195C=	ENSP00000443273.1:p.Ala65=
ENST00000540530.5:n.186C=
ENST00000543289.5:n.685C=
ENST00000545446.5:n.486C=
ENST00000546172.7:c.*191C=	ENSP00000467094.1:n.*191C=
ENST00000546283.5:c.195C=	ENSP00000440348.1:p.Ala65=
ENST00000618074.4:c.195C=	ENSP00000477895.1:p.Ala65=
ENST00000620479.4:c.195C=	ENSP00000480984.1:p.Ala65=
ENST00000622587.4:n.191C=
NM_024407.4:c.195C=	NP_077718.3:p.Ala65=
XM_005259556.3:c.195C=	XP_005259613.2:p.Ala65=
NM_001363602.1:c.195C=	NP_001350531.1:p.Ala65=
XM_017026768.2:c.195C=	XP_016882257.2:p.Ala65=
XM_024451499.1:c.216C=	XP_024307267.1:p.Ala72=
NM_024407.5:c.195C= MANE Select	NP_077718.3:p.Ala65=
NM_001363602.2:c.195C=	NP_001350531.1:p.Ala65=