Canonical Allele Identifier: CA1980452516

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036573_68036577delinsGCTGA , CM000673.2:g.68036573_68036577delinsGCTGA	GRCh38
NC_000011.9:g.67804040_67804044delinsGCTGA , CM000673.1:g.67804040_67804044delinsGCTGA	GRCh37
NC_000011.8:g.67560616_67560620delinsGCTGA	NCBI36
NG_007878.1:g.2558_2562delinsGCTGA , LRG_115:g.2558_2562delinsGCTGA
NG_017040.1:g.10957_10961delinsGCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.613_617delinsGCTGA MANE Select	ENSP00000315774.5:p.Ala205=
ENST00000313468.9:c.613_617delinsGCTGA	ENSP00000315774.5:p.Ala205=
ENST00000524810.5:c.545_549delinsGCTGA
ENST00000528492.1:c.175_179delinsGCTGA	ENSP00000432848.1:p.Ala59=
ENST00000531282.1:n.465_469delinsGCTGA
NM_002496.3:c.613_617delinsGCTGA	NP_002487.1:p.Ala205=
XM_005274013.1:c.613_617delinsGCTGA	XP_005274070.1:p.Ala205=
XM_005274014.1:c.613_617delinsGCTGA	XP_005274071.1:p.Ala205=
XM_005274015.1:c.493_497delinsGCTGA	XP_005274072.1:p.Ala165=
XM_011545053.1:c.613_617delinsGCTGA	XP_011543355.1:p.Ala205=
NM_002496.4:c.613_617delinsGCTGA MANE Select	NP_002487.1:p.Ala205=