Canonical Allele Identifier: CA5977806
Gene: NDUFS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47579300G>T , CM000673.2:g.47579300G>T GRCh38
NC_000011.9:g.47600852G>T , CM000673.1:g.47600852G>T GRCh37
NC_000011.8:g.47557428G>T NCBI36
NG_011946.1:g.5291G>T
NG_011946.2:g.5291G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.99G>T MANE Select ENSP00000263774.4:p.Pro33=
ENST00000531351.2:n.52G>T
ENST00000677462.1:n.68G>T
ENST00000678975.1:n.63G>T
ENST00000263774.8:c.99G>T ENSP00000263774.4:p.Pro33=
ENST00000524568.1:n.202G>T
ENST00000528192.5:c.99G>T ENSP00000432099.1:p.Pro33=
ENST00000529276.1:c.99G>T ENSP00000433753.1:p.Pro33=
ENST00000530295.5:c.67+142G>T ENSP00000431588.1:n.67+142G>T
ENST00000531351.1:n.33G>T
ENST00000533105.1:n.216G>T
ENST00000533507.5:n.816-1225G>T
ENST00000534208.5:c.99G>T ENSP00000433405.1:p.Pro33=
ENST00000534716.2:c.99G>T ENSP00000434970.2:p.Pro33=
NM_004551.2:c.99G>T NP_004542.1:p.Pro33=
NM_004551.3:c.99G>T MANE Select NP_004542.1:p.Pro33=