Canonical Allele Identifier: CA1980447679

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033414C= , CM000673.2:g.68033414C=	GRCh38
NC_000011.9:g.67800881C= , CM000673.1:g.67800881C=	GRCh37
NC_000011.8:g.67557457C=	NCBI36
NG_017040.1:g.7798C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.372+131C= MANE Select	ENSP00000315774.5:n.372+131C=
ENST00000313468.9:c.372+131C=	ENSP00000315774.5:n.372+131C=
ENST00000432321.6:n.620C=
ENST00000524810.5:c.143+131C=
ENST00000525419.5:c.318+131C=	ENSP00000433521.1:n.318+131C=
ENST00000526339.5:c.372+131C=	ENSP00000436287.1:n.372+131C=
ENST00000526446.5:c.*427+131C=	ENSP00000433645.1:n.*427+131C=
ENST00000528492.1:c.-67+2681C=	ENSP00000432848.1:n.-67+2681C=
ENST00000529645.1:c.550+131C=	ENSP00000431293.1:n.550+131C=
ENST00000532399.1:n.1208C=
NM_002496.3:c.372+131C=	NP_002487.1:n.372+131C=
XM_005274013.1:c.372+131C=	XP_005274070.1:n.372+131C=
XM_005274014.1:c.372+131C=	XP_005274071.1:n.372+131C=
XM_005274015.1:c.252+131C=	XP_005274072.1:n.252+131C=
XM_011545053.1:c.372+131C=	XP_011543355.1:n.372+131C=
NM_002496.4:c.372+131C= MANE Select	NP_002487.1:n.372+131C=