Canonical Allele Identifier: CA783450326

Gene: NDUFS7

Linked Data

• dbSNP Id: rs1259776663
• gnomAD v4: 19-1389910-T-G
• MyVariant Identifiers: chr19:g.1389909T>G (hg19) ; chr19:g.1389910T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1389910T>G , CM000681.2:g.1389910T>G	GRCh38
NC_000019.9:g.1389909T>G , CM000681.1:g.1389909T>G	GRCh37
NC_000019.8:g.1340909T>G	NCBI36
NG_008283.1:g.11027T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.229-961T>G MANE Select	ENSP00000233627.9:n.229-961T>G
ENST00000233627.13:c.229-961T>G	ENSP00000233627.9:n.229-961T>G
ENST00000313408.11:c.229-961T>G	ENSP00000364262.5:n.229-961T>G
ENST00000414651.3:c.319-961T>G	ENSP00000406630.2:n.319-961T>G
ENST00000436115.6:n.1223T>G
ENST00000534853.5:c.*23-961T>G	ENSP00000442822.1:n.*23-961T>G
ENST00000535382.1:n.481-961T>G
ENST00000538523.5:n.285-961T>G
ENST00000538662.5:n.256-961T>G
ENST00000538929.5:n.319-961T>G
ENST00000539480.5:c.229-961T>G	ENSP00000443273.1:n.229-961T>G
ENST00000540530.5:n.220-961T>G
ENST00000543289.5:n.719-961T>G
ENST00000545446.5:n.520-961T>G
ENST00000546172.7:c.*225-961T>G	ENSP00000467094.1:n.*225-961T>G
ENST00000546283.5:c.229-961T>G	ENSP00000440348.1:n.229-961T>G
ENST00000618074.4:c.229-961T>G	ENSP00000477895.1:n.229-961T>G
ENST00000620479.4:c.229-961T>G	ENSP00000480984.1:n.229-961T>G
ENST00000622587.4:n.225-961T>G
NM_024407.4:c.229-961T>G	NP_077718.3:n.229-961T>G
XM_005259556.3:c.229-961T>G	XP_005259613.2:n.229-961T>G
NM_001363602.1:c.229-961T>G	NP_001350531.1:n.229-961T>G
XM_024451499.1:c.250-961T>G	XP_024307267.1:n.250-961T>G
NM_024407.5:c.229-961T>G MANE Select	NP_077718.3:n.229-961T>G
NM_001363602.2:c.229-961T>G	NP_001350531.1:n.229-961T>G