Canonical Allele Identifier: CA1980446641

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033048G= , CM000673.2:g.68033048G=	GRCh38
NC_000011.9:g.67800515G= , CM000673.1:g.67800515G=	GRCh37
NC_000011.8:g.67557091G=	NCBI36
NG_017040.1:g.7432G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.199+36G= MANE Select	ENSP00000315774.5:n.199+36G=
ENST00000313468.9:c.199+36G=	ENSP00000315774.5:n.199+36G=
ENST00000432321.6:n.316+36G=
ENST00000453471.6:c.199+36G=	ENSP00000403972.2:n.199+36G=
ENST00000525419.5:c.145+36G=	ENSP00000433521.1:n.145+36G=
ENST00000525628.1:c.199+36G=	ENSP00000432968.1:n.199+36G=
ENST00000526339.5:c.199+36G=	ENSP00000436287.1:n.199+36G=
ENST00000526446.5:c.*254+36G=	ENSP00000433645.1:n.*254+36G=
ENST00000528492.1:c.-67+2315G=	ENSP00000432848.1:n.-67+2315G=
ENST00000529645.1:c.377+36G=	ENSP00000431293.1:n.377+36G=
ENST00000531228.1:c.*41+36G=	ENSP00000433054.1:n.*41+36G=
ENST00000532399.1:n.842G=
NM_002496.3:c.199+36G=	NP_002487.1:n.199+36G=
XM_005274013.1:c.199+36G=	XP_005274070.1:n.199+36G=
XM_005274014.1:c.199+36G=	XP_005274071.1:n.199+36G=
XM_005274015.1:c.79+36G=	XP_005274072.1:n.79+36G=
XM_011545053.1:c.199+36G=	XP_011543355.1:n.199+36G=
NM_002496.4:c.199+36G= MANE Select	NP_002487.1:n.199+36G=