Canonical Allele Identifier: CA402985038

Gene: NDUFS7

Linked Data

• MyVariant Identifiers: chr19:g.1390996G>T (hg19) ; chr19:g.1390997G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1390997G>T , CM000681.2:g.1390997G>T	GRCh38
NC_000019.9:g.1390996G>T , CM000681.1:g.1390996G>T	GRCh37
NC_000019.8:g.1341996G>T	NCBI36
NG_008283.1:g.12114G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.355G>T MANE Select	ENSP00000233627.9:p.Val119Phe
ENST00000233627.13:c.355G>T	ENSP00000233627.9:p.Val119Phe
ENST00000313408.11:c.355G>T	ENSP00000364262.5:p.Val119Phe
ENST00000414651.3:c.445G>T	ENSP00000406630.2:p.Val149Phe
ENST00000436115.6:n.2310G>T
ENST00000534853.5:c.*149G>T	ENSP00000442822.1:n.*149G>T
ENST00000535382.1:n.607G>T
ENST00000538523.5:n.411G>T
ENST00000538662.5:n.382G>T
ENST00000538929.5:n.445G>T
ENST00000539480.5:c.355G>T	ENSP00000443273.1:p.Val119Phe
ENST00000540530.5:n.346G>T
ENST00000543289.5:n.845G>T
ENST00000545446.5:n.646G>T
ENST00000546172.7:c.*351G>T	ENSP00000467094.1:n.*351G>T
ENST00000546283.5:c.355G>T	ENSP00000440348.1:p.Val119Phe
ENST00000618074.4:c.355G>T	ENSP00000477895.1:p.Val119Phe
ENST00000620479.4:c.355G>T	ENSP00000480984.1:p.Val119Phe
ENST00000622587.4:n.351G>T
NM_024407.4:c.355G>T	NP_077718.3:p.Val119Phe
XM_005259556.3:c.355G>T	XP_005259613.2:p.Val119Phe
NM_001363602.1:c.355G>T	NP_001350531.1:p.Val119Phe
XM_024451499.1:c.376G>T	XP_024307267.1:p.Val126Phe
NM_024407.5:c.355G>T MANE Select	NP_077718.3:p.Val119Phe
NM_001363602.2:c.355G>T	NP_001350531.1:p.Val119Phe