Canonical Allele Identifier: CA2792527944
Gene: NDUFS8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68036360del , CM000673.2:g.68036360del GRCh38
NC_000011.9:g.67803827del , CM000673.1:g.67803827del GRCh37
NC_000011.8:g.67560403del NCBI36
NG_007878.1:g.2345del , LRG_115:g.2345del
NG_017040.1:g.10744del

Transcript Alleles

HGVS Amino-acid Change
ENST00000313468.10:c.480del MANE Select ENSP00000315774.5:p.Val162TrpfsTer?
ENST00000313468.9:c.480del ENSP00000315774.5:p.Val162TrpfsTer?
ENST00000524810.5:c.412del
ENST00000526339.5:c.480del ENSP00000436287.1:p.Val162TrpfsTer?
ENST00000526446.5:c.*535del ENSP00000433645.1:n.*535del
ENST00000528492.1:c.42del ENSP00000432848.1:p.Val16TrpfsTer?
ENST00000531282.1:n.332del
NM_002496.3:c.480del NP_002487.1:p.Val162TrpfsTer?
XM_005274013.1:c.480del XP_005274070.1:p.Val162TrpfsTer?
XM_005274014.1:c.480del XP_005274071.1:p.Val162TrpfsTer?
XM_005274015.1:c.360del XP_005274072.1:p.Val122TrpfsTer?
XM_011545053.1:c.480del XP_011543355.1:p.Val162TrpfsTer?
NM_002496.4:c.480del MANE Select NP_002487.1:p.Val162TrpfsTer?