Canonical Allele Identifier: CA1980451833

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036256A= , CM000673.2:g.68036256A=	GRCh38
NC_000011.9:g.67803723A= , CM000673.1:g.67803723A=	GRCh37
NC_000011.8:g.67560299A=	NCBI36
NG_007878.1:g.2241A= , LRG_115:g.2241A=
NG_017040.1:g.10640A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.376A= MANE Select	ENSP00000315774.5:p.Ile126=
ENST00000313468.9:c.376A=	ENSP00000315774.5:p.Ile126=
ENST00000524810.5:c.308A=
ENST00000525419.5:c.322A=	ENSP00000433521.1:p.Ile108=
ENST00000526339.5:c.376A=	ENSP00000436287.1:p.Ile126=
ENST00000526446.5:c.*431A=	ENSP00000433645.1:n.*431A=
ENST00000526542.1:n.327A=
ENST00000528492.1:c.-63A=	ENSP00000432848.1:n.-63A=
ENST00000531282.1:n.228A=
NM_002496.3:c.376A=	NP_002487.1:p.Ile126=
XM_005274013.1:c.376A=	XP_005274070.1:p.Ile126=
XM_005274014.1:c.376A=	XP_005274071.1:p.Ile126=
XM_005274015.1:c.256A=	XP_005274072.1:p.Ile86=
XM_011545053.1:c.376A=	XP_011543355.1:p.Ile126=
NM_002496.4:c.376A= MANE Select	NP_002487.1:p.Ile126=