Canonical Allele Identifier: CA321211

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68032291C>T , CM000673.2:g.68032291C>T	GRCh38
NC_000011.9:g.67799758C>T , CM000673.1:g.67799758C>T	GRCh37
NC_000011.8:g.67556334C>T	NCBI36
NG_017040.1:g.6675C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002496.4:c.64C>T MANE Select	NP_002487.1:p.Pro22Ser
ENST00000313468.10:c.64C>T MANE Select	ENSP00000315774.5:p.Pro22Ser
NM_002496.3:c.64C>T	NP_002487.1:p.Pro22Ser
ENST00000313468.9:c.64C>T	ENSP00000315774.5:p.Pro22Ser
ENST00000432321.6:n.181C>T
ENST00000453471.6:c.64C>T	ENSP00000403972.2:p.Pro22Ser
ENST00000525419.5:c.56-632C>T	ENSP00000433521.1:n.56-632C>T
ENST00000525628.1:c.64C>T	ENSP00000432968.1:p.Pro22Ser
ENST00000526339.5:c.64C>T	ENSP00000436287.1:p.Pro22Ser
ENST00000526446.5:c.64C>T	ENSP00000433645.1:p.Pro22Ser
ENST00000528492.1:c.-67+1558C>T	ENSP00000432848.1:n.-67+1558C>T
ENST00000529645.1:c.55C>T	ENSP00000431293.1:p.Pro19Ser
ENST00000531228.1:c.119C>T	ENSP00000433054.1:p.Ser40Phe
ENST00000531796.1:n.221C>T
ENST00000532399.1:n.85C>T
XM_005274013.1:c.64C>T	XP_005274070.1:p.Pro22Ser
XM_005274014.1:c.64C>T	XP_005274071.1:p.Pro22Ser
XM_005274015.1:c.-244C>T	XP_005274072.1:n.-244C>T
XM_011545053.1:c.64C>T	XP_011543355.1:p.Pro22Ser