Canonical Allele Identifier: CA1980446306

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68032941A= , CM000673.2:g.68032941A=	GRCh38
NC_000011.9:g.67800408A= , CM000673.1:g.67800408A=	GRCh37
NC_000011.8:g.67556984A=	NCBI36
NG_017040.1:g.7325A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.128A= MANE Select	ENSP00000315774.5:p.Asp43=
ENST00000313468.9:c.128A=	ENSP00000315774.5:p.Asp43=
ENST00000432321.6:n.245A=
ENST00000453471.6:c.128A=	ENSP00000403972.2:p.Asp43=
ENST00000525419.5:c.74A=	ENSP00000433521.1:p.Asp25=
ENST00000525628.1:c.128A=	ENSP00000432968.1:p.Asp43=
ENST00000526339.5:c.128A=	ENSP00000436287.1:p.Asp43=
ENST00000526446.5:c.*183A=	ENSP00000433645.1:n.*183A=
ENST00000528492.1:c.-67+2208A=	ENSP00000432848.1:n.-67+2208A=
ENST00000529645.1:c.306A=	ENSP00000431293.1:n.306A=
ENST00000531228.1:c.183A=	ENSP00000433054.1:p.Gly61=
ENST00000532399.1:n.735A=
NM_002496.3:c.128A=	NP_002487.1:p.Asp43=
XM_005274013.1:c.128A=	XP_005274070.1:p.Asp43=
XM_005274014.1:c.128A=	XP_005274071.1:p.Asp43=
XM_005274015.1:c.8A=	XP_005274072.1:p.Asp3=
XM_011545053.1:c.128A=	XP_011543355.1:p.Asp43=
NM_002496.4:c.128A= MANE Select	NP_002487.1:p.Asp43=