Canonical Allele Identifier: CA1586829119

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140647615T= , CM000667.2:g.140647615T= GRCh38
NC_000005.9:g.140027200T= , CM000667.1:g.140027200T= GRCh37
NC_000005.8:g.140007384T= NCBI36
NG_021417.1:g.5171A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252102.9:c.-32A= (NDUFA2) MANE Select ENSP00000252102.5:n.-32A=
ENST00000252102.8:c.-32A= (NDUFA2) ENSP00000252102.4:n.-32A=
ENST00000502960.1:n.157A= (NDUFA2)
ENST00000512088.1:c.-32A= (NDUFA2) ENSP00000427220.1:n.-32A=
ENST00000513256.5:c.4+306T= (IK) ENSP00000425564.1:n.4+306T=
NM_001185012.1:c.-32A= (NDUFA2) NP_001171941.1:n.-32A=
NM_002488.4:c.-32A= (NDUFA2) NP_002479.1:n.-32A=
NR_033697.1:n.171A= (NDUFA2)
NM_002488.5:c.-32A= (NDUFA2) MANE Select NP_002479.1:n.-32A=
NM_001185012.2:c.-32A= (NDUFA2) NP_001171941.1:n.-32A=
NR_033697.2:n.16A= (NDUFA2)