Canonical Allele Identifier: CA1980447744

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033439G= , CM000673.2:g.68033439G=	GRCh38
NC_000011.9:g.67800906G= , CM000673.1:g.67800906G=	GRCh37
NC_000011.8:g.67557482G=	NCBI36
NG_017040.1:g.7823G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.372+156G= MANE Select	ENSP00000315774.5:n.372+156G=
ENST00000313468.9:c.372+156G=	ENSP00000315774.5:n.372+156G=
ENST00000432321.6:n.645G=
ENST00000524810.5:c.143+156G=
ENST00000525419.5:c.318+156G=	ENSP00000433521.1:n.318+156G=
ENST00000526339.5:c.372+156G=	ENSP00000436287.1:n.372+156G=
ENST00000526446.5:c.*427+156G=	ENSP00000433645.1:n.*427+156G=
ENST00000528492.1:c.-67+2706G=	ENSP00000432848.1:n.-67+2706G=
ENST00000529645.1:c.550+156G=	ENSP00000431293.1:n.550+156G=
ENST00000532399.1:n.1233G=
NM_002496.3:c.372+156G=	NP_002487.1:n.372+156G=
XM_005274013.1:c.372+156G=	XP_005274070.1:n.372+156G=
XM_005274014.1:c.372+156G=	XP_005274071.1:n.372+156G=
XM_005274015.1:c.252+156G=	XP_005274072.1:n.252+156G=
XM_011545053.1:c.372+156G=	XP_011543355.1:n.372+156G=
NM_002496.4:c.372+156G= MANE Select	NP_002487.1:n.372+156G=