Canonical Allele Identifier: CA1363288995
Gene: NDUFAF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49022478A= , CM000665.2:g.49022478A= GRCh38
NC_000003.11:g.49059911A= , CM000665.1:g.49059911A= GRCh37
NC_000003.10:g.49034915A= NCBI36
NG_012091.1:g.11965T=
NG_016282.1:g.7004A=
NG_033126.1:g.3594T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326925.11:c.210A= MANE Select ENSP00000323076.5:p.Ile70=
ENST00000326912.8:c.39A= ENSP00000323003.4:p.Ile13=
ENST00000326925.10:c.210A= ENSP00000323076.5:p.Ile70=
ENST00000395458.6:c.39A= ENSP00000378843.2:p.Ile13=
ENST00000451378.2:c.39A= ENSP00000402465.2:p.Ile13=
ENST00000480392.1:n.234A=
ENST00000496152.1:n.366A=
NM_199069.1:c.210A= NP_951032.1:p.Ile70=
NM_199070.1:c.39A= NP_951033.1:p.Ile13=
NM_199073.1:c.39A= NP_951047.1:p.Ile13=
NM_199074.1:c.39A= NP_951056.1:p.Ile13=
NM_199069.2:c.210A= MANE Select NP_951032.1:p.Ile70=
NM_199070.2:c.39A= NP_951033.1:p.Ile13=
NM_199073.2:c.39A= NP_951047.1:p.Ile13=
NM_199074.2:c.39A= NP_951056.1:p.Ile13=