Canonical Allele Identifier: CA1980451845

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036264C= , CM000673.2:g.68036264C=	GRCh38
NC_000011.9:g.67803731C= , CM000673.1:g.67803731C=	GRCh37
NC_000011.8:g.67560307C=	NCBI36
NG_007878.1:g.2249C= , LRG_115:g.2249C=
NG_017040.1:g.10648C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.384C= MANE Select	ENSP00000315774.5:p.Ile128=
ENST00000313468.9:c.384C=	ENSP00000315774.5:p.Ile128=
ENST00000524810.5:c.316C=
ENST00000525419.5:c.330C=	ENSP00000433521.1:p.Ile110=
ENST00000526339.5:c.384C=	ENSP00000436287.1:p.Ile128=
ENST00000526446.5:c.*439C=	ENSP00000433645.1:n.*439C=
ENST00000526542.1:n.335C=
ENST00000528492.1:c.-55C=	ENSP00000432848.1:n.-55C=
ENST00000531282.1:n.236C=
NM_002496.3:c.384C=	NP_002487.1:p.Ile128=
XM_005274013.1:c.384C=	XP_005274070.1:p.Ile128=
XM_005274014.1:c.384C=	XP_005274071.1:p.Ile128=
XM_005274015.1:c.264C=	XP_005274072.1:p.Ile88=
XM_011545053.1:c.384C=	XP_011543355.1:p.Ile128=
NM_002496.4:c.384C= MANE Select	NP_002487.1:p.Ile128=