Canonical Allele Identifier: CA352727446
Gene: NDUFAF3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49022401A>C , CM000665.2:g.49022401A>C GRCh38
NC_000003.11:g.49059834A>C , CM000665.1:g.49059834A>C GRCh37
NC_000003.10:g.49034838A>C NCBI36
NG_012091.1:g.12042T>G
NG_016282.1:g.6927A>C
NG_033126.1:g.3671T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000326925.11:c.133A>C MANE Select ENSP00000323076.5:p.Thr45Pro
ENST00000326912.8:c.-39A>C ENSP00000323003.4:n.-39A>C
ENST00000326925.10:c.133A>C ENSP00000323076.5:p.Thr45Pro
ENST00000395458.6:c.-39A>C ENSP00000378843.2:n.-39A>C
ENST00000451378.2:c.-39A>C ENSP00000402465.2:n.-39A>C
ENST00000480392.1:n.157A>C
ENST00000496152.1:n.289A>C
NM_199069.1:c.133A>C NP_951032.1:p.Thr45Pro
NM_199070.1:c.-39A>C NP_951033.1:n.-39A>C
NM_199073.1:c.-39A>C NP_951047.1:n.-39A>C
NM_199074.1:c.-39A>C NP_951056.1:n.-39A>C
NM_199069.2:c.133A>C MANE Select NP_951032.1:p.Thr45Pro
NM_199070.2:c.-39A>C NP_951033.1:n.-39A>C
NM_199073.2:c.-39A>C NP_951047.1:n.-39A>C
NM_199074.2:c.-39A>C NP_951056.1:n.-39A>C