Canonical Allele Identifier: CA402985826

Gene: NDUFS7

Linked Data

• MyVariant Identifiers: chr19:g.1391132G>A (hg19) ; chr19:g.1391133G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1391133G>A , CM000681.2:g.1391133G>A	GRCh38
NC_000019.9:g.1391132G>A , CM000681.1:g.1391132G>A	GRCh37
NC_000019.8:g.1342132G>A	NCBI36
NG_008283.1:g.12250G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.423G>A MANE Select	ENSP00000233627.9:p.Met141Ile
ENST00000233627.13:c.423G>A	ENSP00000233627.9:p.Met141Ile
ENST00000313408.11:c.423G>A	ENSP00000364262.5:p.Met141Ile
ENST00000414651.3:c.513G>A	ENSP00000406630.2:p.Met171Ile
ENST00000436115.6:n.2378G>A
ENST00000534853.5:c.*217G>A	ENSP00000442822.1:n.*217G>A
ENST00000535382.1:n.675G>A
ENST00000538523.5:n.479G>A
ENST00000538662.5:n.518G>A
ENST00000538929.5:n.513G>A
ENST00000539480.5:c.423G>A	ENSP00000443273.1:p.Met141Ile
ENST00000540530.5:n.414G>A
ENST00000543289.5:n.981G>A
ENST00000545446.5:n.714G>A
ENST00000546172.7:c.*419G>A	ENSP00000467094.1:n.*419G>A
ENST00000546283.5:c.423G>A	ENSP00000440348.1:p.Met141Ile
ENST00000618074.4:c.430G>A	ENSP00000477895.1:p.Ala144Thr
ENST00000620479.4:c.427G>A	ENSP00000480984.1:p.Ala143Thr
ENST00000622587.4:n.487G>A
NM_024407.4:c.423G>A	NP_077718.3:p.Met141Ile
XM_005259556.3:c.423G>A	XP_005259613.2:p.Met141Ile
NM_001363602.1:c.423G>A	NP_001350531.1:p.Met141Ile
XM_024451499.1:c.444G>A	XP_024307267.1:p.Met148Ile
NM_024407.5:c.423G>A MANE Select	NP_077718.3:p.Met141Ile
NM_001363602.2:c.423G>A	NP_001350531.1:p.Met141Ile