Canonical Allele Identifier: CA504715429

Gene: NDUFS7

Linked Data

• MyVariant Identifiers: chr19:g.1388877C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1388878C>G , CM000681.2:g.1388878C>G	GRCh38
NC_000019.9:g.1388877C>G , CM000681.1:g.1388877C>G	GRCh37
NC_000019.8:g.1339877C>G	NCBI36
NG_008283.1:g.9995C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.168C>G MANE Select	ENSP00000233627.9:p.Pro56=
ENST00000233627.13:c.168C>G	ENSP00000233627.9:p.Pro56=
ENST00000313408.11:c.168C>G	ENSP00000364262.5:p.Pro56=
ENST00000414651.3:c.258C>G	ENSP00000406630.2:p.Pro86=
ENST00000436115.6:n.191C>G
ENST00000534853.5:c.163C>G	ENSP00000442822.1:p.Gln55Glu
ENST00000535382.1:n.420C>G
ENST00000538523.5:n.224C>G
ENST00000538662.5:n.195C>G
ENST00000538929.5:n.258C>G
ENST00000539480.5:c.168C>G	ENSP00000443273.1:p.Pro56=
ENST00000540530.5:n.159C>G
ENST00000543289.5:n.658C>G
ENST00000545446.5:n.459C>G
ENST00000546172.7:c.*164C>G	ENSP00000467094.1:n.*164C>G
ENST00000546283.5:c.168C>G	ENSP00000440348.1:p.Pro56=
ENST00000618074.4:c.168C>G	ENSP00000477895.1:p.Pro56=
ENST00000620479.4:c.168C>G	ENSP00000480984.1:p.Pro56=
ENST00000622587.4:n.164C>G
NM_024407.4:c.168C>G	NP_077718.3:p.Pro56=
XM_005259556.3:c.168C>G	XP_005259613.2:p.Pro56=
NM_001363602.1:c.168C>G	NP_001350531.1:p.Pro56=
XM_017026768.2:c.168C>G	XP_016882257.2:p.Pro56=
XM_024451499.1:c.189C>G	XP_024307267.1:p.Pro63=
NM_024407.5:c.168C>G MANE Select	NP_077718.3:p.Pro56=
NM_001363602.2:c.168C>G	NP_001350531.1:p.Pro56=