Canonical Allele Identifier: CA1980451939

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036337T= , CM000673.2:g.68036337T=	GRCh38
NC_000011.9:g.67803804T= , CM000673.1:g.67803804T=	GRCh37
NC_000011.8:g.67560380T=	NCBI36
NG_007878.1:g.2322T= , LRG_115:g.2322T=
NG_017040.1:g.10721T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.457T= MANE Select	ENSP00000315774.5:p.Cys153=
ENST00000313468.9:c.457T=	ENSP00000315774.5:p.Cys153=
ENST00000524810.5:c.389T=
ENST00000525419.5:c.403T=	ENSP00000433521.1:p.Cys135=
ENST00000526339.5:c.457T=	ENSP00000436287.1:p.Cys153=
ENST00000526446.5:c.*512T=	ENSP00000433645.1:n.*512T=
ENST00000528492.1:c.19T=	ENSP00000432848.1:p.Cys7=
ENST00000531282.1:n.309T=
NM_002496.3:c.457T=	NP_002487.1:p.Cys153=
XM_005274013.1:c.457T=	XP_005274070.1:p.Cys153=
XM_005274014.1:c.457T=	XP_005274071.1:p.Cys153=
XM_005274015.1:c.337T=	XP_005274072.1:p.Cys113=
XM_011545053.1:c.457T=	XP_011543355.1:p.Cys153=
NM_002496.4:c.457T= MANE Select	NP_002487.1:p.Cys153=