Canonical Allele Identifier: CA2614691414

Gene: NDUFS8

Linked Data

• gnomAD v4: 11-68036193-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036193G>A , CM000673.2:g.68036193G>A	GRCh38
NC_000011.9:g.67803660G>A , CM000673.1:g.67803660G>A	GRCh37
NC_000011.8:g.67560236G>A	NCBI36
NG_007878.1:g.2178G>A , LRG_115:g.2178G>A
NG_017040.1:g.10577G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000313468.10:c.373-60G>A MANE Select	ENSP00000315774.5:n.373-60G>A
ENST00000313468.9:c.373-60G>A	ENSP00000315774.5:n.373-60G>A
ENST00000524810.5:c.305-60G>A
ENST00000525419.5:c.319-60G>A	ENSP00000433521.1:n.319-60G>A
ENST00000526339.5:c.373-60G>A	ENSP00000436287.1:n.373-60G>A
ENST00000526446.5:c.*428-60G>A	ENSP00000433645.1:n.*428-60G>A
ENST00000526542.1:n.324-60G>A
ENST00000528492.1:c.-66-60G>A	ENSP00000432848.1:n.-66-60G>A
ENST00000531282.1:n.165G>A
NM_002496.3:c.373-60G>A	NP_002487.1:n.373-60G>A
XM_005274013.1:c.373-60G>A	XP_005274070.1:n.373-60G>A
XM_005274014.1:c.373-60G>A	XP_005274071.1:n.373-60G>A
XM_005274015.1:c.253-60G>A	XP_005274072.1:n.253-60G>A
XM_011545053.1:c.373-60G>A	XP_011543355.1:n.373-60G>A
NM_002496.4:c.373-60G>A MANE Select	NP_002487.1:n.373-60G>A