Canonical Allele Identifier: CA1980447135

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033227T= , CM000673.2:g.68033227T=	GRCh38
NC_000011.9:g.67800694T= , CM000673.1:g.67800694T=	GRCh37
NC_000011.8:g.67557270T=	NCBI36
NG_017040.1:g.7611T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.316T= MANE Select	ENSP00000315774.5:p.Ser106=
ENST00000313468.9:c.316T=	ENSP00000315774.5:p.Ser106=
ENST00000432321.6:n.433T=
ENST00000453471.6:c.316T=	ENSP00000403972.2:p.Ser106=
ENST00000524810.5:c.87T=
ENST00000525419.5:c.262T=	ENSP00000433521.1:p.Ser88=
ENST00000525628.1:c.316T=	ENSP00000432968.1:p.Ser106=
ENST00000526339.5:c.316T=	ENSP00000436287.1:p.Ser106=
ENST00000526446.5:c.*371T=	ENSP00000433645.1:n.*371T=
ENST00000528492.1:c.-67+2494T=	ENSP00000432848.1:n.-67+2494T=
ENST00000529645.1:c.494T=	ENSP00000431293.1:n.494T=
ENST00000532399.1:n.1021T=
NM_002496.3:c.316T=	NP_002487.1:p.Ser106=
XM_005274013.1:c.316T=	XP_005274070.1:p.Ser106=
XM_005274014.1:c.316T=	XP_005274071.1:p.Ser106=
XM_005274015.1:c.196T=	XP_005274072.1:p.Ser66=
XM_011545053.1:c.316T=	XP_011543355.1:p.Ser106=
NM_002496.4:c.316T= MANE Select	NP_002487.1:p.Ser106=