Canonical Allele Identifier: CA2614693280

Gene: NDUFS8

Linked Data

• gnomAD v4: 11-68036633-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036633A>T , CM000673.2:g.68036633A>T	GRCh38
NC_000011.9:g.67804100A>T , CM000673.1:g.67804100A>T	GRCh37
NC_000011.8:g.67560676A>T	NCBI36
NG_007878.1:g.2618A>T , LRG_115:g.2618A>T
NG_017040.1:g.11017A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.*40A>T MANE Select	ENSP00000315774.5:n.*40A>T
ENST00000313468.9:c.*40A>T	ENSP00000315774.5:n.*40A>T
ENST00000524810.5:c.605A>T
ENST00000528492.1:c.*40A>T	ENSP00000432848.1:n.*40A>T
ENST00000531282.1:n.525A>T
NM_002496.3:c.*40A>T	NP_002487.1:n.*40A>T
XM_005274013.1:c.*40A>T	XP_005274070.1:n.*40A>T
XM_005274014.1:c.*40A>T	XP_005274071.1:n.*40A>T
XM_005274015.1:c.*40A>T	XP_005274072.1:n.*40A>T
XM_011545053.1:c.*40A>T	XP_011543355.1:n.*40A>T
NM_002496.4:c.*40A>T MANE Select	NP_002487.1:n.*40A>T