Canonical Allele Identifier: CA504895196

Gene: NDUFS7

Linked Data

• MyVariant Identifiers: chr19:g.1391046C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1391047C>A , CM000681.2:g.1391047C>A	GRCh38
NC_000019.9:g.1391046C>A , CM000681.1:g.1391046C>A	GRCh37
NC_000019.8:g.1342046C>A	NCBI36
NG_008283.1:g.12164C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.405C>A MANE Select	ENSP00000233627.9:p.Arg135=
ENST00000233627.13:c.405C>A	ENSP00000233627.9:p.Arg135=
ENST00000313408.11:c.405C>A	ENSP00000364262.5:p.Arg135=
ENST00000414651.3:c.495C>A	ENSP00000406630.2:p.Arg165=
ENST00000436115.6:n.2360C>A
ENST00000534853.5:c.*199C>A	ENSP00000442822.1:n.*199C>A
ENST00000535382.1:n.657C>A
ENST00000538523.5:n.461C>A
ENST00000538662.5:n.432C>A
ENST00000538929.5:n.495C>A
ENST00000539480.5:c.405C>A	ENSP00000443273.1:p.Arg135=
ENST00000540530.5:n.396C>A
ENST00000543289.5:n.895C>A
ENST00000545446.5:n.696C>A
ENST00000546172.7:c.*401C>A	ENSP00000467094.1:n.*401C>A
ENST00000546283.5:c.405C>A	ENSP00000440348.1:p.Arg135=
ENST00000618074.4:c.405C>A	ENSP00000477895.1:p.Arg135=
ENST00000620479.4:c.405C>A	ENSP00000480984.1:p.Arg135=
ENST00000622587.4:n.401C>A
NM_024407.4:c.405C>A	NP_077718.3:p.Arg135=
XM_005259556.3:c.405C>A	XP_005259613.2:p.Arg135=
NM_001363602.1:c.405C>A	NP_001350531.1:p.Arg135=
XM_024451499.1:c.426C>A	XP_024307267.1:p.Arg142=
NM_024407.5:c.405C>A MANE Select	NP_077718.3:p.Arg135=
NM_001363602.2:c.405C>A	NP_001350531.1:p.Arg135=