Canonical Allele Identifier: CA1980446770

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033083_68033084delinsCT , CM000673.2:g.68033083_68033084delinsCT	GRCh38
NC_000011.9:g.67800550_67800551delinsCT , CM000673.1:g.67800550_67800551delinsCT	GRCh37
NC_000011.8:g.67557126_67557127delinsCT	NCBI36
NG_017040.1:g.7467_7468delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.200-28_200-27delinsCT MANE Select	ENSP00000315774.5:n.200-28_200-27delinsCT
ENST00000313468.9:c.200-28_200-27delinsCT	ENSP00000315774.5:n.200-28_200-27delinsCT
ENST00000432321.6:n.317-28_317-27delinsCT
ENST00000453471.6:c.200-28_200-27delinsCT	ENSP00000403972.2:n.200-28_200-27delinsCT
ENST00000525419.5:c.146-28_146-27delinsCT	ENSP00000433521.1:n.146-28_146-27delinsCT
ENST00000525628.1:c.200-28_200-27delinsCT	ENSP00000432968.1:n.200-28_200-27delinsCT
ENST00000526339.5:c.200-28_200-27delinsCT	ENSP00000436287.1:n.200-28_200-27delinsCT
ENST00000526446.5:c.*255-28_*255-27delinsCT	ENSP00000433645.1:n.*255-28_*255-27delinsCT
ENST00000528492.1:c.-67+2350_-67+2351delinsCT	ENSP00000432848.1:n.-67+2350_-67+2351delinsCT
ENST00000529645.1:c.378-28_378-27delinsCT	ENSP00000431293.1:n.378-28_378-27delinsCT
ENST00000531228.1:c.*42-28_*42-27delinsCT	ENSP00000433054.1:n.*42-28_*42-27delinsCT
ENST00000532399.1:n.877_878delinsCT
NM_002496.3:c.200-28_200-27delinsCT	NP_002487.1:n.200-28_200-27delinsCT
XM_005274013.1:c.200-28_200-27delinsCT	XP_005274070.1:n.200-28_200-27delinsCT
XM_005274014.1:c.200-28_200-27delinsCT	XP_005274071.1:n.200-28_200-27delinsCT
XM_005274015.1:c.80-28_80-27delinsCT	XP_005274072.1:n.80-28_80-27delinsCT
XM_011545053.1:c.200-28_200-27delinsCT	XP_011543355.1:n.200-28_200-27delinsCT
NM_002496.4:c.200-28_200-27delinsCT MANE Select	NP_002487.1:n.200-28_200-27delinsCT