Canonical Allele Identifier: CA2317693301

Gene: NDUFS7

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1388864G= , CM000681.2:g.1388864G=	GRCh38
NC_000019.9:g.1388863G= , CM000681.1:g.1388863G=	GRCh37
NC_000019.8:g.1339863G=	NCBI36
NG_008283.1:g.9981G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.154G= MANE Select	ENSP00000233627.9:p.Val52=
ENST00000233627.13:c.154G=	ENSP00000233627.9:p.Val52=
ENST00000313408.11:c.154G=	ENSP00000364262.5:p.Val52=
ENST00000414651.3:c.244G=	ENSP00000406630.2:p.Val82=
ENST00000436115.6:n.177G=
ENST00000534853.5:c.149G=	ENSP00000442822.1:p.Arg50=
ENST00000535382.1:n.406G=
ENST00000538523.5:n.210G=
ENST00000538662.5:n.181G=
ENST00000538929.5:n.244G=
ENST00000539480.5:c.154G=	ENSP00000443273.1:p.Val52=
ENST00000540530.5:n.145G=
ENST00000543289.5:n.644G=
ENST00000545446.5:n.445G=
ENST00000546172.7:c.*150G=	ENSP00000467094.1:n.*150G=
ENST00000546283.5:c.154G=	ENSP00000440348.1:p.Val52=
ENST00000618074.4:c.154G=	ENSP00000477895.1:p.Val52=
ENST00000620479.4:c.154G=	ENSP00000480984.1:p.Val52=
ENST00000622587.4:n.150G=
NM_024407.4:c.154G=	NP_077718.3:p.Val52=
XM_005259556.3:c.154G=	XP_005259613.2:p.Val52=
NM_001363602.1:c.154G=	NP_001350531.1:p.Val52=
XM_017026768.2:c.154G=	XP_016882257.2:p.Val52=
XM_024451499.1:c.175G=	XP_024307267.1:p.Val59=
NM_024407.5:c.154G= MANE Select	NP_077718.3:p.Val52=
NM_001363602.2:c.154G=	NP_001350531.1:p.Val52=