Canonical Allele Identifier: CA1980452357

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036509C= , CM000673.2:g.68036509C=	GRCh38
NC_000011.9:g.67803976C= , CM000673.1:g.67803976C=	GRCh37
NC_000011.8:g.67560552C=	NCBI36
NG_007878.1:g.2494C= , LRG_115:g.2494C=
NG_017040.1:g.10893C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.549C= MANE Select	ENSP00000315774.5:p.Tyr183=
ENST00000313468.9:c.549C=	ENSP00000315774.5:p.Tyr183=
ENST00000524810.5:c.481C=
ENST00000526339.5:c.549C=	ENSP00000436287.1:p.Tyr183=
ENST00000526446.5:c.*604C=	ENSP00000433645.1:n.*604C=
ENST00000528492.1:c.111C=	ENSP00000432848.1:p.Tyr37=
ENST00000531282.1:n.401C=
NM_002496.3:c.549C=	NP_002487.1:p.Tyr183=
XM_005274013.1:c.549C=	XP_005274070.1:p.Tyr183=
XM_005274014.1:c.549C=	XP_005274071.1:p.Tyr183=
XM_005274015.1:c.429C=	XP_005274072.1:p.Tyr143=
XM_011545053.1:c.549C=	XP_011543355.1:p.Tyr183=
NM_002496.4:c.549C= MANE Select	NP_002487.1:p.Tyr183=