Canonical Allele Identifier: CA2675613222

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140647610_140647611insATGTAGC , CM000667.2:g.140647610_140647611insATGTAGC GRCh38
NC_000005.9:g.140027195_140027196insATGTAGC , CM000667.1:g.140027195_140027196insATGTAGC GRCh37
NC_000005.8:g.140007379_140007380insATGTAGC NCBI36
NG_021417.1:g.5176_5177insCTACATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252102.9:c.-27_-26insCTACATG (NDUFA2) MANE Select ENSP00000252102.5:n.-27_-26insCTACATG
ENST00000252102.8:c.-27_-26insCTACATG (NDUFA2) ENSP00000252102.4:n.-27_-26insCTACATG
ENST00000502960.1:n.162_163insCTACATG (NDUFA2)
ENST00000512088.1:c.-27_-26insCTACATG (NDUFA2) ENSP00000427220.1:n.-27_-26insCTACATG
ENST00000513256.5:c.4+301_4+302insATGTAGC (IK) ENSP00000425564.1:n.4+301_4+302insATGTAGC
NM_001185012.1:c.-27_-26insCTACATG (NDUFA2) NP_001171941.1:n.-27_-26insCTACATG
NM_002488.4:c.-27_-26insCTACATG (NDUFA2) NP_002479.1:n.-27_-26insCTACATG
NR_033697.1:n.176_177insCTACATG (NDUFA2)
NM_002488.5:c.-27_-26insCTACATG (NDUFA2) MANE Select NP_002479.1:n.-27_-26insCTACATG
NM_001185012.2:c.-27_-26insCTACATG (NDUFA2) NP_001171941.1:n.-27_-26insCTACATG
NR_033697.2:n.21_22insCTACATG (NDUFA2)