Canonical Allele Identifier: CA1363289068
Gene: NDUFAF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49022565_49022567delinsCTG , CM000665.2:g.49022565_49022567delinsCTG GRCh38
NC_000003.11:g.49059998_49060000delinsCTG , CM000665.1:g.49059998_49060000delinsCTG GRCh37
NC_000003.10:g.49035002_49035004delinsCTG NCBI36
NG_012091.1:g.11876_11878delinsCAG
NG_016282.1:g.7091_7093delinsCTG
NG_033126.1:g.3505_3507delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000326925.11:c.270+27_270+29delinsCTG MANE Select ENSP00000323076.5:n.270+27_270+29delinsCTG
ENST00000326912.8:c.99+27_99+29delinsCTG ENSP00000323003.4:n.99+27_99+29delinsCTG
ENST00000326925.10:c.270+27_270+29delinsCTG ENSP00000323076.5:n.270+27_270+29delinsCTG
ENST00000395458.6:c.99+27_99+29delinsCTG ENSP00000378843.2:n.99+27_99+29delinsCTG
ENST00000451378.2:c.99+27_99+29delinsCTG ENSP00000402465.2:n.99+27_99+29delinsCTG
ENST00000480392.1:n.294+27_294+29delinsCTG
ENST00000496152.1:n.426+27_426+29delinsCTG
NM_199069.1:c.270+27_270+29delinsCTG NP_951032.1:n.270+27_270+29delinsCTG
NM_199070.1:c.99+27_99+29delinsCTG NP_951033.1:n.99+27_99+29delinsCTG
NM_199073.1:c.99+27_99+29delinsCTG NP_951047.1:n.99+27_99+29delinsCTG
NM_199074.1:c.99+27_99+29delinsCTG NP_951056.1:n.99+27_99+29delinsCTG
NM_199069.2:c.270+27_270+29delinsCTG MANE Select NP_951032.1:n.270+27_270+29delinsCTG
NM_199070.2:c.99+27_99+29delinsCTG NP_951033.1:n.99+27_99+29delinsCTG
NM_199073.2:c.99+27_99+29delinsCTG NP_951047.1:n.99+27_99+29delinsCTG
NM_199074.2:c.99+27_99+29delinsCTG NP_951056.1:n.99+27_99+29delinsCTG