Canonical Allele Identifier: CA2838438548
Gene: NDUFS8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68036637dup , CM000673.2:g.68036637dup GRCh38
NC_000011.9:g.67804104dup , CM000673.1:g.67804104dup GRCh37
NC_000011.8:g.67560680dup NCBI36
NG_007878.1:g.2622dup , LRG_115:g.2622dup
NG_017040.1:g.11021dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000313468.10:c.*44dup MANE Select ENSP00000315774.5:n.*44dup
ENST00000313468.9:c.*44dup ENSP00000315774.5:n.*44dup
ENST00000524810.5:c.609dup
ENST00000528492.1:c.*44dup ENSP00000432848.1:n.*44dup
ENST00000531282.1:n.529dup
NM_002496.3:c.*44dup NP_002487.1:n.*44dup
XM_005274013.1:c.*44dup XP_005274070.1:n.*44dup
XM_005274014.1:c.*44dup XP_005274071.1:n.*44dup
XM_005274015.1:c.*44dup XP_005274072.1:n.*44dup
XM_011545053.1:c.*44dup XP_011543355.1:n.*44dup
NM_002496.4:c.*44dup MANE Select NP_002487.1:n.*44dup