Canonical Allele Identifier: CA1363288928

Gene: NDUFAF3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49022455T= , CM000665.2:g.49022455T=	GRCh38
NC_000003.11:g.49059888T= , CM000665.1:g.49059888T=	GRCh37
NC_000003.10:g.49034892T=	NCBI36
NG_012091.1:g.11988A=
NG_016282.1:g.6981T=
NG_033126.1:g.3617A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326925.11:c.187T= MANE Select	ENSP00000323076.5:p.Tyr63=
ENST00000326912.8:c.16T=	ENSP00000323003.4:p.Tyr6=
ENST00000326925.10:c.187T=	ENSP00000323076.5:p.Tyr63=
ENST00000395458.6:c.16T=	ENSP00000378843.2:p.Tyr6=
ENST00000451378.2:c.16T=	ENSP00000402465.2:p.Tyr6=
ENST00000480392.1:n.211T=
ENST00000496152.1:n.343T=
NM_199069.1:c.187T=	NP_951032.1:p.Tyr63=
NM_199070.1:c.16T=	NP_951033.1:p.Tyr6=
NM_199073.1:c.16T=	NP_951047.1:p.Tyr6=
NM_199074.1:c.16T=	NP_951056.1:p.Tyr6=
NM_199069.2:c.187T= MANE Select	NP_951032.1:p.Tyr63=
NM_199070.2:c.16T=	NP_951033.1:p.Tyr6=
NM_199073.2:c.16T=	NP_951047.1:p.Tyr6=
NM_199074.2:c.16T=	NP_951056.1:p.Tyr6=