Canonical Allele Identifier: CA1586829132

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140647623C= , CM000667.2:g.140647623C= GRCh38
NC_000005.9:g.140027208C= , CM000667.1:g.140027208C= GRCh37
NC_000005.8:g.140007392C= NCBI36
NG_021417.1:g.5163G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252102.9:c.-40G= (NDUFA2) MANE Select ENSP00000252102.5:n.-40G=
ENST00000252102.8:c.-40G= (NDUFA2) ENSP00000252102.4:n.-40G=
ENST00000502960.1:n.149G= (NDUFA2)
ENST00000512088.1:c.-40G= (NDUFA2) ENSP00000427220.1:n.-40G=
ENST00000513256.5:c.4+314C= (IK) ENSP00000425564.1:n.4+314C=
NM_001185012.1:c.-40G= (NDUFA2) NP_001171941.1:n.-40G=
NM_002488.4:c.-40G= (NDUFA2) NP_002479.1:n.-40G=
NR_033697.1:n.163G= (NDUFA2)
NM_002488.5:c.-40G= (NDUFA2) MANE Select NP_002479.1:n.-40G=
NM_001185012.2:c.-40G= (NDUFA2) NP_001171941.1:n.-40G=
NR_033697.2:n.8G= (NDUFA2)