Canonical Allele Identifier: CA2574899199

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036446G>C , CM000673.2:g.68036446G>C	GRCh38
NC_000011.9:g.67803913G>C , CM000673.1:g.67803913G>C	GRCh37
NC_000011.8:g.67560489G>C	NCBI36
NG_007878.1:g.2431G>C , LRG_115:g.2431G>C
NG_017040.1:g.10830G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.502-16G>C MANE Select	ENSP00000315774.5:n.502-16G>C
ENST00000313468.9:c.502-16G>C	ENSP00000315774.5:n.502-16G>C
ENST00000524810.5:c.434-16G>C
ENST00000526339.5:c.502-16G>C	ENSP00000436287.1:n.502-16G>C
ENST00000526446.5:c.*557-16G>C	ENSP00000433645.1:n.*557-16G>C
ENST00000528492.1:c.64-16G>C	ENSP00000432848.1:n.64-16G>C
ENST00000531282.1:n.354-16G>C
NM_002496.3:c.502-16G>C	NP_002487.1:n.502-16G>C
XM_005274013.1:c.502-16G>C	XP_005274070.1:n.502-16G>C
XM_005274014.1:c.502-16G>C	XP_005274071.1:n.502-16G>C
XM_005274015.1:c.382-16G>C	XP_005274072.1:n.382-16G>C
XM_011545053.1:c.502-16G>C	XP_011543355.1:n.502-16G>C
NM_002496.4:c.502-16G>C MANE Select	NP_002487.1:n.502-16G>C