Canonical Allele Identifier: CA2582636649

Gene: NDUFS7

Linked Data

• gnomAD v4: 19-1389737-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1389737A>T , CM000681.2:g.1389737A>T	GRCh38
NC_000019.9:g.1389736A>T , CM000681.1:g.1389736A>T	GRCh37
NC_000019.8:g.1340736A>T	NCBI36
NG_008283.1:g.10854A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.228+799A>T MANE Select	ENSP00000233627.9:n.228+799A>T
ENST00000233627.13:c.228+799A>T	ENSP00000233627.9:n.228+799A>T
ENST00000313408.11:c.228+799A>T	ENSP00000364262.5:n.228+799A>T
ENST00000414651.3:c.318+799A>T	ENSP00000406630.2:n.318+799A>T
ENST00000436115.6:n.1050A>T
ENST00000534853.5:c.*22+799A>T	ENSP00000442822.1:n.*22+799A>T
ENST00000535382.1:n.480+799A>T
ENST00000538523.5:n.284+799A>T
ENST00000538662.5:n.255+799A>T
ENST00000538929.5:n.318+799A>T
ENST00000539480.5:c.228+799A>T	ENSP00000443273.1:n.228+799A>T
ENST00000540530.5:n.219+799A>T
ENST00000543289.5:n.718+799A>T
ENST00000545446.5:n.519+799A>T
ENST00000546172.7:c.*224+799A>T	ENSP00000467094.1:n.*224+799A>T
ENST00000546283.5:c.228+799A>T	ENSP00000440348.1:n.228+799A>T
ENST00000618074.4:c.228+799A>T	ENSP00000477895.1:n.228+799A>T
ENST00000620479.4:c.228+799A>T	ENSP00000480984.1:n.228+799A>T
ENST00000622587.4:n.224+799A>T
NM_024407.4:c.228+799A>T	NP_077718.3:n.228+799A>T
XM_005259556.3:c.228+799A>T	XP_005259613.2:n.228+799A>T
NM_001363602.1:c.228+799A>T	NP_001350531.1:n.228+799A>T
XM_024451499.1:c.249+799A>T	XP_024307267.1:n.249+799A>T
NM_024407.5:c.228+799A>T MANE Select	NP_077718.3:n.228+799A>T
NM_001363602.2:c.228+799A>T	NP_001350531.1:n.228+799A>T