Canonical Allele Identifier: CA304059740

Gene: NDUFS7

Linked Data

• dbSNP Id: rs1037386000
• gnomAD v2: 19-1391285-G-A
• gnomAD v3: 19-1391286-G-A
• gnomAD v4: 19-1391286-G-A
• MyVariant Identifiers: chr19:g.1391285G>A (hg19) ; chr19:g.1391286G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1391286G>A , CM000681.2:g.1391286G>A	GRCh38
NC_000019.9:g.1391285G>A , CM000681.1:g.1391285G>A	GRCh37
NC_000019.8:g.1342285G>A	NCBI36
NG_008283.1:g.12403G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.455+121G>A MANE Select	ENSP00000233627.9:n.455+121G>A
ENST00000233627.13:c.455+121G>A	ENSP00000233627.9:n.455+121G>A
ENST00000313408.11:c.455+121G>A	ENSP00000364262.5:n.455+121G>A
ENST00000414651.3:c.545+121G>A	ENSP00000406630.2:n.545+121G>A
ENST00000436115.6:n.2410+121G>A
ENST00000534853.5:c.*249+121G>A	ENSP00000442822.1:n.*249+121G>A
ENST00000535382.1:n.707+121G>A
ENST00000538523.5:n.511+121G>A
ENST00000538662.5:n.550+121G>A
ENST00000538929.5:n.545+121G>A
ENST00000539480.5:c.455+121G>A	ENSP00000443273.1:n.455+121G>A
ENST00000540530.5:n.446+121G>A
ENST00000543289.5:n.1013+121G>A
ENST00000545446.5:n.746+121G>A
ENST00000546172.7:c.*451+121G>A	ENSP00000467094.1:n.*451+121G>A
ENST00000546283.5:c.455+121G>A	ENSP00000440348.1:n.455+121G>A
ENST00000618074.4:c.462+121G>A	ENSP00000477895.1:n.462+121G>A
ENST00000620479.4:c.459+121G>A	ENSP00000480984.1:n.459+121G>A
ENST00000622587.4:n.519+121G>A
NM_024407.4:c.455+121G>A	NP_077718.3:n.455+121G>A
XM_005259556.3:c.455+121G>A	XP_005259613.2:n.455+121G>A
NM_001363602.1:c.455+121G>A	NP_001350531.1:n.455+121G>A
XM_024451499.1:c.476+121G>A	XP_024307267.1:n.476+121G>A
NM_024407.5:c.455+121G>A MANE Select	NP_077718.3:n.455+121G>A
NM_001363602.2:c.455+121G>A	NP_001350531.1:n.455+121G>A