Canonical Allele Identifier: CA1363288820

Gene: NDUFAF3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49022399G= , CM000665.2:g.49022399G=	GRCh38
NC_000003.11:g.49059832G= , CM000665.1:g.49059832G=	GRCh37
NC_000003.10:g.49034836G=	NCBI36
NG_012091.1:g.12044C=
NG_016282.1:g.6925G=
NG_033126.1:g.3673C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326925.11:c.131G= MANE Select	ENSP00000323076.5:p.Arg44=
ENST00000326912.8:c.-41G=	ENSP00000323003.4:n.-41G=
ENST00000326925.10:c.131G=	ENSP00000323076.5:p.Arg44=
ENST00000395458.6:c.-41G=	ENSP00000378843.2:n.-41G=
ENST00000451378.2:c.-41G=	ENSP00000402465.2:n.-41G=
ENST00000480392.1:n.155G=
ENST00000496152.1:n.287G=
NM_199069.1:c.131G=	NP_951032.1:p.Arg44=
NM_199070.1:c.-41G=	NP_951033.1:n.-41G=
NM_199073.1:c.-41G=	NP_951047.1:n.-41G=
NM_199074.1:c.-41G=	NP_951056.1:n.-41G=
NM_199069.2:c.131G= MANE Select	NP_951032.1:p.Arg44=
NM_199070.2:c.-41G=	NP_951033.1:n.-41G=
NM_199073.2:c.-41G=	NP_951047.1:n.-41G=
NM_199074.2:c.-41G=	NP_951056.1:n.-41G=