Canonical Allele Identifier: CA9043344

Gene: NDUFS7

Linked Data

• dbSNP Id: rs756557024
• ExAC: 19:1391011 G / A
• gnomAD v2: 19-1391011-G-A
• gnomAD v4: 19-1391012-G-A
• MyVariant Identifiers: chr19:g.1391011G>A (hg19) ; chr19:g.1391012G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1391012G>A , CM000681.2:g.1391012G>A	GRCh38
NC_000019.9:g.1391011G>A , CM000681.1:g.1391011G>A	GRCh37
NC_000019.8:g.1342011G>A	NCBI36
NG_008283.1:g.12129G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.370G>A MANE Select	ENSP00000233627.9:p.Gly124Ser
ENST00000233627.13:c.370G>A	ENSP00000233627.9:p.Gly124Ser
ENST00000313408.11:c.370G>A	ENSP00000364262.5:p.Gly124Ser
ENST00000414651.3:c.460G>A	ENSP00000406630.2:p.Gly154Ser
ENST00000436115.6:n.2325G>A
ENST00000534853.5:c.*164G>A	ENSP00000442822.1:n.*164G>A
ENST00000535382.1:n.622G>A
ENST00000538523.5:n.426G>A
ENST00000538662.5:n.397G>A
ENST00000538929.5:n.460G>A
ENST00000539480.5:c.370G>A	ENSP00000443273.1:p.Gly124Ser
ENST00000540530.5:n.361G>A
ENST00000543289.5:n.860G>A
ENST00000545446.5:n.661G>A
ENST00000546172.7:c.*366G>A	ENSP00000467094.1:n.*366G>A
ENST00000546283.5:c.370G>A	ENSP00000440348.1:p.Gly124Ser
ENST00000618074.4:c.370G>A	ENSP00000477895.1:p.Gly124Ser
ENST00000620479.4:c.370G>A	ENSP00000480984.1:p.Gly124Ser
ENST00000622587.4:n.366G>A
NM_024407.4:c.370G>A	NP_077718.3:p.Gly124Ser
XM_005259556.3:c.370G>A	XP_005259613.2:p.Gly124Ser
NM_001363602.1:c.370G>A	NP_001350531.1:p.Gly124Ser
XM_024451499.1:c.391G>A	XP_024307267.1:p.Gly131Ser
NM_024407.5:c.370G>A MANE Select	NP_077718.3:p.Gly124Ser
NM_001363602.2:c.370G>A	NP_001350531.1:p.Gly124Ser