Canonical Allele Identifier: CA1980451910

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036321G= , CM000673.2:g.68036321G=	GRCh38
NC_000011.9:g.67803788G= , CM000673.1:g.67803788G=	GRCh37
NC_000011.8:g.67560364G=	NCBI36
NG_007878.1:g.2306G= , LRG_115:g.2306G=
NG_017040.1:g.10705G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.441G= MANE Select	ENSP00000315774.5:p.Met147=
ENST00000313468.9:c.441G=	ENSP00000315774.5:p.Met147=
ENST00000524810.5:c.373G=
ENST00000525419.5:c.387G=	ENSP00000433521.1:p.Met129=
ENST00000526339.5:c.441G=	ENSP00000436287.1:p.Met147=
ENST00000526446.5:c.*496G=	ENSP00000433645.1:n.*496G=
ENST00000528492.1:c.3G=	ENSP00000432848.1:p.Met1=
ENST00000531282.1:n.293G=
NM_002496.3:c.441G=	NP_002487.1:p.Met147=
XM_005274013.1:c.441G=	XP_005274070.1:p.Met147=
XM_005274014.1:c.441G=	XP_005274071.1:p.Met147=
XM_005274015.1:c.321G=	XP_005274072.1:p.Met107=
XM_011545053.1:c.441G=	XP_011543355.1:p.Met147=
NM_002496.4:c.441G= MANE Select	NP_002487.1:p.Met147=