Canonical Allele Identifier: CA1586829245

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140647636T= , CM000667.2:g.140647636T= GRCh38
NC_000005.9:g.140027221T= , CM000667.1:g.140027221T= GRCh37
NC_000005.8:g.140007405T= NCBI36
NG_021417.1:g.5150A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252102.8:c.-53A= (NDUFA2) ENSP00000252102.4:n.-53A=
ENST00000502960.1:n.136A= (NDUFA2)
ENST00000512088.1:c.-53A= (NDUFA2) ENSP00000427220.1:n.-53A=
ENST00000513256.5:c.4+327T= (IK) ENSP00000425564.1:n.4+327T=
NM_001185012.1:c.-53A= (NDUFA2) NP_001171941.1:n.-53A=
NM_002488.4:c.-53A= (NDUFA2) NP_002479.1:n.-53A=
NR_033697.1:n.150A= (NDUFA2)