Canonical Allele Identifier: CA323264
Gene: NDUFA2 HGNC NCBI
TMCO6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140645607C>T , CM000667.2:g.140645607C>T GRCh38
NC_000005.9:g.140025192C>T , CM000667.1:g.140025192C>T GRCh37
NC_000005.8:g.140005376C>T NCBI36
NG_021417.1:g.7179G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252102.9:c.280G>A (NDUFA2) MANE Select ENSP00000252102.5:p.Val94Ile
ENST00000252102.8:c.280G>A (NDUFA2) ENSP00000252102.4:p.Val94Ile
ENST00000502960.1:n.588G>A (NDUFA2)
ENST00000510680.1:n.59+1649G>A (NDUFA2)
ENST00000512088.1:c.*96G>A (NDUFA2) ENSP00000427220.1:n.*96G>A
NM_001185012.1:c.*96G>A (NDUFA2) NP_001171941.1:n.*96G>A
NM_002488.4:c.280G>A (NDUFA2) NP_002479.1:p.Val94Ile
NR_033697.1:n.602G>A (NDUFA2)
XM_011537663.1:c.1219-1208C>T (TMCO6) XP_011535965.1:n.1219-1208C>T
XM_011537663.2:c.1219-1208C>T (TMCO6) XP_011535965.1:n.1219-1208C>T
NM_002488.5:c.280G>A (NDUFA2) MANE Select NP_002479.1:p.Val94Ile
NM_001185012.2:c.*96G>A (NDUFA2) NP_001171941.1:n.*96G>A
NR_033697.2:n.447G>A (NDUFA2)