Canonical Allele Identifier: CA2675613230

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140647613_140647614insAT , CM000667.2:g.140647613_140647614insAT GRCh38
NC_000005.9:g.140027198_140027199insAT , CM000667.1:g.140027198_140027199insAT GRCh37
NC_000005.8:g.140007382_140007383insAT NCBI36
NG_021417.1:g.5172_5173insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252102.9:c.-31_-30insAT (NDUFA2) MANE Select ENSP00000252102.5:n.-31_-30insAT
ENST00000252102.8:c.-31_-30insAT (NDUFA2) ENSP00000252102.4:n.-31_-30insAT
ENST00000502960.1:n.158_159insAT (NDUFA2)
ENST00000512088.1:c.-31_-30insAT (NDUFA2) ENSP00000427220.1:n.-31_-30insAT
ENST00000513256.5:c.4+304_4+305insAT (IK) ENSP00000425564.1:n.4+304_4+305insAT
NM_001185012.1:c.-31_-30insAT (NDUFA2) NP_001171941.1:n.-31_-30insAT
NM_002488.4:c.-31_-30insAT (NDUFA2) NP_002479.1:n.-31_-30insAT
NR_033697.1:n.172_173insAT (NDUFA2)
NM_002488.5:c.-31_-30insAT (NDUFA2) MANE Select NP_002479.1:n.-31_-30insAT
NM_001185012.2:c.-31_-30insAT (NDUFA2) NP_001171941.1:n.-31_-30insAT
NR_033697.2:n.17_18insAT (NDUFA2)