Canonical Allele Identifier: CA2317693310

Gene: NDUFS7

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1388873A= , CM000681.2:g.1388873A=	GRCh38
NC_000019.9:g.1388872A= , CM000681.1:g.1388872A=	GRCh37
NC_000019.8:g.1339872A=	NCBI36
NG_008283.1:g.9990A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.163A= MANE Select	ENSP00000233627.9:p.Lys55=
ENST00000233627.13:c.163A=	ENSP00000233627.9:p.Lys55=
ENST00000313408.11:c.163A=	ENSP00000364262.5:p.Lys55=
ENST00000414651.3:c.253A=	ENSP00000406630.2:p.Lys85=
ENST00000436115.6:n.186A=
ENST00000534853.5:c.158A=	ENSP00000442822.1:p.Gln53=
ENST00000535382.1:n.415A=
ENST00000538523.5:n.219A=
ENST00000538662.5:n.190A=
ENST00000538929.5:n.253A=
ENST00000539480.5:c.163A=	ENSP00000443273.1:p.Lys55=
ENST00000540530.5:n.154A=
ENST00000543289.5:n.653A=
ENST00000545446.5:n.454A=
ENST00000546172.7:c.*159A=	ENSP00000467094.1:n.*159A=
ENST00000546283.5:c.163A=	ENSP00000440348.1:p.Lys55=
ENST00000618074.4:c.163A=	ENSP00000477895.1:p.Lys55=
ENST00000620479.4:c.163A=	ENSP00000480984.1:p.Lys55=
ENST00000622587.4:n.159A=
NM_024407.4:c.163A=	NP_077718.3:p.Lys55=
XM_005259556.3:c.163A=	XP_005259613.2:p.Lys55=
NM_001363602.1:c.163A=	NP_001350531.1:p.Lys55=
XM_017026768.2:c.163A=	XP_016882257.2:p.Lys55=
XM_024451499.1:c.184A=	XP_024307267.1:p.Lys62=
NM_024407.5:c.163A= MANE Select	NP_077718.3:p.Lys55=
NM_001363602.2:c.163A=	NP_001350531.1:p.Lys55=