Canonical Allele Identifier: CA504715455

Gene: NDUFS7

Linked Data

• MyVariant Identifiers: chr19:g.1388901G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1388902G>T , CM000681.2:g.1388902G>T	GRCh38
NC_000019.9:g.1388901G>T , CM000681.1:g.1388901G>T	GRCh37
NC_000019.8:g.1339901G>T	NCBI36
NG_008283.1:g.10019G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.192G>T MANE Select	ENSP00000233627.9:p.Val64=
ENST00000233627.13:c.192G>T	ENSP00000233627.9:p.Val64=
ENST00000313408.11:c.192G>T	ENSP00000364262.5:p.Val64=
ENST00000414651.3:c.282G>T	ENSP00000406630.2:p.Val94=
ENST00000436115.6:n.215G>T
ENST00000534853.5:c.187G>T	ENSP00000442822.1:p.Gly63Cys
ENST00000535382.1:n.444G>T
ENST00000538523.5:n.248G>T
ENST00000538662.5:n.219G>T
ENST00000538929.5:n.282G>T
ENST00000539480.5:c.192G>T	ENSP00000443273.1:p.Val64=
ENST00000540530.5:n.183G>T
ENST00000543289.5:n.682G>T
ENST00000545446.5:n.483G>T
ENST00000546172.7:c.*188G>T	ENSP00000467094.1:n.*188G>T
ENST00000546283.5:c.192G>T	ENSP00000440348.1:p.Val64=
ENST00000618074.4:c.192G>T	ENSP00000477895.1:p.Val64=
ENST00000620479.4:c.192G>T	ENSP00000480984.1:p.Val64=
ENST00000622587.4:n.188G>T
NM_024407.4:c.192G>T	NP_077718.3:p.Val64=
XM_005259556.3:c.192G>T	XP_005259613.2:p.Val64=
NM_001363602.1:c.192G>T	NP_001350531.1:p.Val64=
XM_017026768.2:c.192G>T	XP_016882257.2:p.Val64=
XM_024451499.1:c.213G>T	XP_024307267.1:p.Val71=
NM_024407.5:c.192G>T MANE Select	NP_077718.3:p.Val64=
NM_001363602.2:c.192G>T	NP_001350531.1:p.Val64=