Canonical Allele Identifier: CA1586829076

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140647594_140647600delinsATCGAAG , CM000667.2:g.140647594_140647600delinsATCGAAG GRCh38
NC_000005.9:g.140027179_140027185delinsATCGAAG , CM000667.1:g.140027179_140027185delinsATCGAAG GRCh37
NC_000005.8:g.140007363_140007369delinsATCGAAG NCBI36
NG_021417.1:g.5186_5192delinsCTTCGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252102.9:c.-17_-11delinsCTTCGAT (NDUFA2) MANE Select ENSP00000252102.5:n.-17_-11delinsCTTCGAT
ENST00000252102.8:c.-17_-11delinsCTTCGAT (NDUFA2) ENSP00000252102.4:n.-17_-11delinsCTTCGAT
ENST00000502960.1:n.172_178delinsCTTCGAT (NDUFA2)
ENST00000512088.1:c.-17_-11delinsCTTCGAT (NDUFA2) ENSP00000427220.1:n.-17_-11delinsCTTCGAT
ENST00000513256.5:c.4+285_4+291delinsATCGAAG (IK) ENSP00000425564.1:n.4+285_4+291delinsATCGAAG
NM_001185012.1:c.-17_-11delinsCTTCGAT (NDUFA2) NP_001171941.1:n.-17_-11delinsCTTCGAT
NM_002488.4:c.-17_-11delinsCTTCGAT (NDUFA2) NP_002479.1:n.-17_-11delinsCTTCGAT
NR_033697.1:n.186_192delinsCTTCGAT (NDUFA2)
NM_002488.5:c.-17_-11delinsCTTCGAT (NDUFA2) MANE Select NP_002479.1:n.-17_-11delinsCTTCGAT
NM_001185012.2:c.-17_-11delinsCTTCGAT (NDUFA2) NP_001171941.1:n.-17_-11delinsCTTCGAT
NR_033697.2:n.31_37delinsCTTCGAT (NDUFA2)