Canonical Allele Identifier: CA1363288810
Gene: NDUFAF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49022397G= , CM000665.2:g.49022397G= GRCh38
NC_000003.11:g.49059830G= , CM000665.1:g.49059830G= GRCh37
NC_000003.10:g.49034834G= NCBI36
NG_012091.1:g.12046C=
NG_016282.1:g.6923G=
NG_033126.1:g.3675C=

Transcript Alleles

HGVS Amino-acid change
ENST00000326925.11:c.129G= MANE Select ENSP00000323076.5:p.Gln43=
ENST00000326912.8:c.-43G= ENSP00000323003.4:n.-43G=
ENST00000326925.10:c.129G= ENSP00000323076.5:p.Gln43=
ENST00000395458.6:c.-43G= ENSP00000378843.2:n.-43G=
ENST00000451378.2:c.-43G= ENSP00000402465.2:n.-43G=
ENST00000480392.1:n.153G=
ENST00000496152.1:n.285G=
NM_199069.1:c.129G= NP_951032.1:p.Gln43=
NM_199070.1:c.-43G= NP_951033.1:n.-43G=
NM_199073.1:c.-43G= NP_951047.1:n.-43G=
NM_199074.1:c.-43G= NP_951056.1:n.-43G=
NM_199069.2:c.129G= MANE Select NP_951032.1:p.Gln43=
NM_199070.2:c.-43G= NP_951033.1:n.-43G=
NM_199073.2:c.-43G= NP_951047.1:n.-43G=
NM_199074.2:c.-43G= NP_951056.1:n.-43G=