Canonical Allele Identifier: CA1980452185

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036495G= , CM000673.2:g.68036495G=	GRCh38
NC_000011.9:g.67803962G= , CM000673.1:g.67803962G=	GRCh37
NC_000011.8:g.67560538G=	NCBI36
NG_007878.1:g.2480G= , LRG_115:g.2480G=
NG_017040.1:g.10879G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.535G= MANE Select	ENSP00000315774.5:p.Glu179=
ENST00000313468.9:c.535G=	ENSP00000315774.5:p.Glu179=
ENST00000524810.5:c.467G=
ENST00000526339.5:c.535G=	ENSP00000436287.1:p.Glu179=
ENST00000526446.5:c.*590G=	ENSP00000433645.1:n.*590G=
ENST00000528492.1:c.97G=	ENSP00000432848.1:p.Glu33=
ENST00000531282.1:n.387G=
NM_002496.3:c.535G=	NP_002487.1:p.Glu179=
XM_005274013.1:c.535G=	XP_005274070.1:p.Glu179=
XM_005274014.1:c.535G=	XP_005274071.1:p.Glu179=
XM_005274015.1:c.415G=	XP_005274072.1:p.Glu139=
XM_011545053.1:c.535G=	XP_011543355.1:p.Glu179=
NM_002496.4:c.535G= MANE Select	NP_002487.1:p.Glu179=