Canonical Allele Identifier: CA1586828816

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140647541C= , CM000667.2:g.140647541C= GRCh38
NC_000005.9:g.140027126C= , CM000667.1:g.140027126C= GRCh37
NC_000005.8:g.140007310C= NCBI36
NG_021417.1:g.5245G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252102.9:c.43G= (NDUFA2) MANE Select ENSP00000252102.5:p.Gly15=
ENST00000252102.8:c.43G= (NDUFA2) ENSP00000252102.4:p.Gly15=
ENST00000502960.1:n.231G= (NDUFA2)
ENST00000512088.1:c.43G= (NDUFA2) ENSP00000427220.1:p.Gly15=
ENST00000513256.5:c.4+232C= (IK) ENSP00000425564.1:n.4+232C=
NM_001185012.1:c.43G= (NDUFA2) NP_001171941.1:p.Gly15=
NM_002488.4:c.43G= (NDUFA2) NP_002479.1:p.Gly15=
NR_033697.1:n.245G= (NDUFA2)
NM_002488.5:c.43G= (NDUFA2) MANE Select NP_002479.1:p.Gly15=
NM_001185012.2:c.43G= (NDUFA2) NP_001171941.1:p.Gly15=
NR_033697.2:n.90G= (NDUFA2)