Canonical Allele Identifier: CA2320171547
Gene: NDUFA11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903907_5903909delinsAAG , CM000681.2:g.5903907_5903909delinsAAG GRCh38
NC_000019.9:g.5903918_5903920delinsAAG , CM000681.1:g.5903918_5903920delinsAAG GRCh37
NC_000019.8:g.5854918_5854920delinsAAG NCBI36
NG_027808.1:g.5105_5107delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000591160.1:n.98_100delinsCTT
NM_001193375.1:c.-201_-199delinsCTT NP_001180304.1:n.-201_-199delinsCTT
NM_175614.4:c.-201_-199delinsCTT NP_783313.1:n.-201_-199delinsCTT
NR_034166.2:n.105_107delinsCTT