Canonical Allele Identifier: CA1980452598

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036612C= , CM000673.2:g.68036612C=	GRCh38
NC_000011.9:g.67804079C= , CM000673.1:g.67804079C=	GRCh37
NC_000011.8:g.67560655C=	NCBI36
NG_007878.1:g.2597C= , LRG_115:g.2597C=
NG_017040.1:g.10996C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000313468.10:c.*19C= MANE Select	ENSP00000315774.5:n.*19C=
ENST00000313468.9:c.*19C=	ENSP00000315774.5:n.*19C=
ENST00000524810.5:c.584C=
ENST00000528492.1:c.*19C=	ENSP00000432848.1:n.*19C=
ENST00000531282.1:n.504C=
NM_002496.3:c.*19C=	NP_002487.1:n.*19C=
XM_005274013.1:c.*19C=	XP_005274070.1:n.*19C=
XM_005274014.1:c.*19C=	XP_005274071.1:n.*19C=
XM_005274015.1:c.*19C=	XP_005274072.1:n.*19C=
XM_011545053.1:c.*19C=	XP_011543355.1:n.*19C=
NM_002496.4:c.*19C= MANE Select	NP_002487.1:n.*19C=