Canonical Allele Identifier: CA1363289034

Gene: NDUFAF3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49022530C= , CM000665.2:g.49022530C=	GRCh38
NC_000003.11:g.49059963C= , CM000665.1:g.49059963C=	GRCh37
NC_000003.10:g.49034967C=	NCBI36
NG_012091.1:g.11913G=
NG_016282.1:g.7056C=
NG_033126.1:g.3542G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326925.11:c.262C= MANE Select	ENSP00000323076.5:p.Gln88=
ENST00000326912.8:c.91C=	ENSP00000323003.4:p.Gln31=
ENST00000326925.10:c.262C=	ENSP00000323076.5:p.Gln88=
ENST00000395458.6:c.91C=	ENSP00000378843.2:p.Gln31=
ENST00000451378.2:c.91C=	ENSP00000402465.2:p.Gln31=
ENST00000480392.1:n.286C=
ENST00000496152.1:n.418C=
NM_199069.1:c.262C=	NP_951032.1:p.Gln88=
NM_199070.1:c.91C=	NP_951033.1:p.Gln31=
NM_199073.1:c.91C=	NP_951047.1:p.Gln31=
NM_199074.1:c.91C=	NP_951056.1:p.Gln31=
NM_199069.2:c.262C= MANE Select	NP_951032.1:p.Gln88=
NM_199070.2:c.91C=	NP_951033.1:p.Gln31=
NM_199073.2:c.91C=	NP_951047.1:p.Gln31=
NM_199074.2:c.91C=	NP_951056.1:p.Gln31=