Canonical Allele Identifier: CA304059638

Gene: NDUFS7

Linked Data

• ClinVar Variation Id: 3010728
• ClinVar RCV Id: RCV003862367
• dbSNP Id: rs919687560
• gnomAD v2: 19-1390992-C-T
• gnomAD v3: 19-1390993-C-T
• gnomAD v4: 19-1390993-C-T
• MyVariant Identifiers: chr19:g.1390992C>T (hg19) ; chr19:g.1390993C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1390993C>T , CM000681.2:g.1390993C>T	GRCh38
NC_000019.9:g.1390992C>T , CM000681.1:g.1390992C>T	GRCh37
NC_000019.8:g.1341992C>T	NCBI36
NG_008283.1:g.12110C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.351C>T MANE Select	ENSP00000233627.9:p.Ser117=
ENST00000233627.13:c.351C>T	ENSP00000233627.9:p.Ser117=
ENST00000313408.11:c.351C>T	ENSP00000364262.5:p.Ser117=
ENST00000414651.3:c.441C>T	ENSP00000406630.2:p.Ser147=
ENST00000436115.6:n.2306C>T
ENST00000534853.5:c.*145C>T	ENSP00000442822.1:n.*145C>T
ENST00000535382.1:n.603C>T
ENST00000538523.5:n.407C>T
ENST00000538662.5:n.378C>T
ENST00000538929.5:n.441C>T
ENST00000539480.5:c.351C>T	ENSP00000443273.1:p.Ser117=
ENST00000540530.5:n.342C>T
ENST00000543289.5:n.841C>T
ENST00000545446.5:n.642C>T
ENST00000546172.7:c.*347C>T	ENSP00000467094.1:n.*347C>T
ENST00000546283.5:c.351C>T	ENSP00000440348.1:p.Ser117=
ENST00000618074.4:c.351C>T	ENSP00000477895.1:p.Ser117=
ENST00000620479.4:c.351C>T	ENSP00000480984.1:p.Ser117=
ENST00000622587.4:n.347C>T
NM_024407.4:c.351C>T	NP_077718.3:p.Ser117=
XM_005259556.3:c.351C>T	XP_005259613.2:p.Ser117=
NM_001363602.1:c.351C>T	NP_001350531.1:p.Ser117=
XM_024451499.1:c.372C>T	XP_024307267.1:p.Ser124=
NM_024407.5:c.351C>T MANE Select	NP_077718.3:p.Ser117=
NM_001363602.2:c.351C>T	NP_001350531.1:p.Ser117=