Canonical Allele Identifier: CA402985262

Gene: NDUFS7

Linked Data

• MyVariant Identifiers: chr19:g.1391030T>G (hg19) ; chr19:g.1391031T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1391031T>G , CM000681.2:g.1391031T>G	GRCh38
NC_000019.9:g.1391030T>G , CM000681.1:g.1391030T>G	GRCh37
NC_000019.8:g.1342030T>G	NCBI36
NG_008283.1:g.12148T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.389T>G MANE Select	ENSP00000233627.9:p.Met130Arg
ENST00000233627.13:c.389T>G	ENSP00000233627.9:p.Met130Arg
ENST00000313408.11:c.389T>G	ENSP00000364262.5:p.Met130Arg
ENST00000414651.3:c.479T>G	ENSP00000406630.2:p.Met160Arg
ENST00000436115.6:n.2344T>G
ENST00000534853.5:c.*183T>G	ENSP00000442822.1:n.*183T>G
ENST00000535382.1:n.641T>G
ENST00000538523.5:n.445T>G
ENST00000538662.5:n.416T>G
ENST00000538929.5:n.479T>G
ENST00000539480.5:c.389T>G	ENSP00000443273.1:p.Met130Arg
ENST00000540530.5:n.380T>G
ENST00000543289.5:n.879T>G
ENST00000545446.5:n.680T>G
ENST00000546172.7:c.*385T>G	ENSP00000467094.1:n.*385T>G
ENST00000546283.5:c.389T>G	ENSP00000440348.1:p.Met130Arg
ENST00000618074.4:c.389T>G	ENSP00000477895.1:p.Met130Arg
ENST00000620479.4:c.389T>G	ENSP00000480984.1:p.Met130Arg
ENST00000622587.4:n.385T>G
NM_024407.4:c.389T>G	NP_077718.3:p.Met130Arg
XM_005259556.3:c.389T>G	XP_005259613.2:p.Met130Arg
NM_001363602.1:c.389T>G	NP_001350531.1:p.Met130Arg
XM_024451499.1:c.410T>G	XP_024307267.1:p.Met137Arg
NM_024407.5:c.389T>G MANE Select	NP_077718.3:p.Met130Arg
NM_001363602.2:c.389T>G	NP_001350531.1:p.Met130Arg