Canonical Allele Identifier: CA9831951

Gene: UQCC1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35384111C>T , CM000682.2:g.35384111C>T	GRCh38
NC_000020.10:g.33971914C>T , CM000682.1:g.33971914C>T	GRCh37
NC_000020.9:g.33435328C>T	NCBI36
NG_021421.1:g.33032G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453855.6:c.152G>A	ENSP00000390334.2:p.Arg51Gln
ENST00000374385.10:c.152G>A MANE Select	ENSP00000363506.5:p.Arg51Gln
ENST00000349714.9:c.152G>A	ENSP00000335364.6:p.Arg51Gln
ENST00000359226.6:c.152G>A	ENSP00000352161.2:p.Arg51Gln
ENST00000374380.6:c.130-9855G>A	ENSP00000363501.2:n.130-9855G>A
ENST00000374384.6:c.152G>A	ENSP00000363505.2:p.Arg51Gln
ENST00000374385.9:c.152G>A	ENSP00000363506.5:p.Arg51Gln
ENST00000374394.7:c.*206G>A	ENSP00000363515.3:n.*206G>A
ENST00000397553.6:c.*88G>A	ENSP00000380685.2:n.*88G>A
ENST00000397554.5:c.152G>A	ENSP00000380686.1:p.Arg51Gln
ENST00000397556.7:c.14G>A	ENSP00000380688.4:p.Arg5Gln
ENST00000424405.5:c.130-2086G>A	ENSP00000399713.1:n.130-2086G>A
ENST00000438533.5:c.194G>A	ENSP00000398531.1:p.Arg65Gln
ENST00000443429.5:c.152G>A	ENSP00000416246.1:p.Arg51Gln
ENST00000453855.5:c.149G>A	ENSP00000390334.1:p.Arg50Gln
ENST00000457259.5:c.124+9981G>A
ENST00000491040.5:c.*108-2086G>A	ENSP00000420584.1:n.*108-2086G>A
ENST00000491125.5:n.165G>A
ENST00000495752.1:n.229G>A
NM_001184977.1:c.130-9855G>A	NP_001171906.1:n.130-9855G>A
NM_018244.4:c.152G>A	NP_060714.3:p.Arg51Gln
NM_199487.2:c.152G>A	NP_955781.2:p.Arg51Gln
XM_011528877.1:c.194G>A	XP_011527179.1:p.Arg65Gln
XM_011528878.1:c.130-2086G>A	XP_011527180.1:n.130-2086G>A
XM_011528879.1:c.14G>A	XP_011527181.1:p.Arg5Gln
XM_011528880.1:c.14G>A	XP_011527182.1:p.Arg5Gln
XM_011528881.1:c.-72-2086G>A	XP_011527183.1:n.-72-2086G>A
XM_011528882.1:c.-178G>A	XP_011527184.1:n.-178G>A
XM_011528883.1:c.-104-2086G>A	XP_011527185.1:n.-104-2086G>A
XM_011528884.1:c.-104-2086G>A	XP_011527186.1:n.-104-2086G>A
XM_011528878.2:c.130-2086G>A	XP_011527180.1:n.130-2086G>A
XM_011528880.2:c.14G>A	XP_011527182.1:p.Arg5Gln
XM_011528881.3:c.-72-2086G>A	XP_011527183.1:n.-72-2086G>A
XM_011528882.2:c.-178G>A	XP_011527184.1:n.-178G>A
XM_011528883.2:c.-104-2086G>A	XP_011527185.1:n.-104-2086G>A
XM_011528884.2:c.-104-2086G>A	XP_011527186.1:n.-104-2086G>A
NM_018244.5:c.152G>A MANE Select	NP_060714.3:p.Arg51Gln
NM_001184977.2:c.130-9855G>A	NP_001171906.1:n.130-9855G>A
NM_199487.3:c.152G>A	NP_955781.2:p.Arg51Gln