Canonical Allele Identifier: CA1980446691

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033065_68033066delinsTG , CM000673.2:g.68033065_68033066delinsTG	GRCh38
NC_000011.9:g.67800532_67800533delinsTG , CM000673.1:g.67800532_67800533delinsTG	GRCh37
NC_000011.8:g.67557108_67557109delinsTG	NCBI36
NG_017040.1:g.7449_7450delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.200-46_200-45delinsTG MANE Select	ENSP00000315774.5:n.200-46_200-45delinsTG
ENST00000313468.9:c.200-46_200-45delinsTG	ENSP00000315774.5:n.200-46_200-45delinsTG
ENST00000432321.6:n.317-46_317-45delinsTG
ENST00000453471.6:c.200-46_200-45delinsTG	ENSP00000403972.2:n.200-46_200-45delinsTG
ENST00000525419.5:c.146-46_146-45delinsTG	ENSP00000433521.1:n.146-46_146-45delinsTG
ENST00000525628.1:c.200-46_200-45delinsTG	ENSP00000432968.1:n.200-46_200-45delinsTG
ENST00000526339.5:c.200-46_200-45delinsTG	ENSP00000436287.1:n.200-46_200-45delinsTG
ENST00000526446.5:c.*255-46_*255-45delinsTG	ENSP00000433645.1:n.*255-46_*255-45delinsTG
ENST00000528492.1:c.-67+2332_-67+2333delinsTG	ENSP00000432848.1:n.-67+2332_-67+2333delinsTG
ENST00000529645.1:c.378-46_378-45delinsTG	ENSP00000431293.1:n.378-46_378-45delinsTG
ENST00000531228.1:c.*42-46_*42-45delinsTG	ENSP00000433054.1:n.*42-46_*42-45delinsTG
ENST00000532399.1:n.859_860delinsTG
NM_002496.3:c.200-46_200-45delinsTG	NP_002487.1:n.200-46_200-45delinsTG
XM_005274013.1:c.200-46_200-45delinsTG	XP_005274070.1:n.200-46_200-45delinsTG
XM_005274014.1:c.200-46_200-45delinsTG	XP_005274071.1:n.200-46_200-45delinsTG
XM_005274015.1:c.80-46_80-45delinsTG	XP_005274072.1:n.80-46_80-45delinsTG
XM_011545053.1:c.200-46_200-45delinsTG	XP_011543355.1:n.200-46_200-45delinsTG
NM_002496.4:c.200-46_200-45delinsTG MANE Select	NP_002487.1:n.200-46_200-45delinsTG