Canonical Allele Identifier: CA1803697572

Gene: NDUFAF6 TP53INP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.94948283T= , CM000670.2:g.94948283T=	GRCh38
NC_000008.10:g.95960511T= , CM000670.1:g.95960511T=	GRCh37
NC_000008.9:g.96029687T=	NCBI36
NG_016647.2:g.58013T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521840.2:n.396-9712T= (NDUFAF6)
ENST00000697354.1:n.347-9712T= (NDUFAF6)
ENST00000697355.1:c.-387-9712T= (NDUFAF6)	ENSP00000513277.1:n.-387-9712T=
ENST00000697356.1:n.243+2664T= (NDUFAF6)
ENST00000342697.5:c.-151+871A= (TP53INP1) MANE Select	ENSP00000344215.4:n.-151+871A=
ENST00000342697.4:c.-151+871A= (TP53INP1)	ENSP00000344215.4:n.-151+871A=
ENST00000396113.5:c.-799+2664T= (NDUFAF6)	ENSP00000379419.1:n.-799+2664T=
ENST00000448464.6:c.-151+871A= (TP53INP1)	ENSP00000390063.2:n.-151+871A=
ENST00000519136.5:c.-440-9712T= (NDUFAF6)	ENSP00000429585.1:n.-440-9712T=
ENST00000523378.5:c.-387-9712T= (NDUFAF6)	ENSP00000428034.1:n.-387-9712T=
NM_001135733.1:c.-151+871A= (TP53INP1)	NP_001129205.1:n.-151+871A=
NM_033285.3:c.-151+871A= (TP53INP1)	NP_150601.1:n.-151+871A=
XM_011516835.1:c.-524-9712T= (NDUFAF6)	XP_011515137.1:n.-524-9712T=
NM_001354514.1:c.-485-9712T= (NDUFAF6)	NP_001341443.1:n.-485-9712T=
NM_001354515.1:c.-268-9712T= (NDUFAF6)	NP_001341444.1:n.-268-9712T=
NM_001354516.1:c.-263-9712T= (NDUFAF6)	NP_001341445.1:n.-263-9712T=
NM_001354522.1:c.-687-9712T= (NDUFAF6)	NP_001341451.1:n.-687-9712T=
NM_001354524.1:c.-760-9712T= (NDUFAF6)	NP_001341453.1:n.-760-9712T=
NM_001354525.1:c.-804-9712T= (NDUFAF6)	NP_001341454.1:n.-804-9712T=
NM_001354534.1:c.-321-9712T= (NDUFAF6)	NP_001341463.1:n.-321-9712T=
NR_148903.1:n.161-9712T= (NDUFAF6)
NR_148904.1:n.161-2488T= (NDUFAF6)
NR_148905.1:n.297+2664T= (NDUFAF6)
NR_148906.1:n.297+2664T= (NDUFAF6)
XM_011516835.2:c.-524-9712T= (NDUFAF6)	XP_011515137.1:n.-524-9712T=
XM_017013027.2:c.-525+2664T= (NDUFAF6)	XP_016868516.1:n.-525+2664T=
XM_017013028.1:c.-426-9712T= (NDUFAF6)	XP_016868517.1:n.-426-9712T=
NM_033285.4:c.-151+871A= (TP53INP1) MANE Select	NP_150601.1:n.-151+871A=
NM_001135733.2:c.-151+871A= (TP53INP1)	NP_001129205.1:n.-151+871A=
NR_148903.2:n.130-9712T= (NDUFAF6)
NR_148904.2:n.130-2488T= (NDUFAF6)
NR_148905.2:n.266+2664T= (NDUFAF6)
NR_148906.2:n.266+2664T= (NDUFAF6)
NM_001354514.2:c.-485-9712T= (NDUFAF6)	NP_001341443.1:n.-485-9712T=
NM_001354515.2:c.-268-9712T= (NDUFAF6)	NP_001341444.1:n.-268-9712T=
NM_001354516.2:c.-263-9712T= (NDUFAF6)	NP_001341445.1:n.-263-9712T=
NM_001354522.2:c.-687-9712T= (NDUFAF6)	NP_001341451.1:n.-687-9712T=
NM_001354524.2:c.-760-9712T= (NDUFAF6)	NP_001341453.1:n.-760-9712T=
NM_001354525.2:c.-804-9712T= (NDUFAF6)	NP_001341454.1:n.-804-9712T=
NM_001354534.2:c.-321-9712T= (NDUFAF6)	NP_001341463.1:n.-321-9712T=