Canonical Allele Identifier: CA489983687

Gene: NDUFAF1

Linked Data

• MyVariant Identifiers: chr15:g.41688760A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41396562A>T , CM000677.2:g.41396562A>T	GRCh38
NC_000015.9:g.41688760A>T , CM000677.1:g.41688760A>T	GRCh37
NC_000015.8:g.39476052A>T	NCBI36
NG_031924.1:g.10899T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260361.9:c.498T>A MANE Select	ENSP00000260361.4:p.Thr166=
ENST00000558719.2:c.498T>A	ENSP00000454083.2:p.Thr166=
ENST00000560978.2:c.498T>A	ENSP00000453944.2:p.Thr166=
ENST00000676533.1:c.498T>A	ENSP00000504040.1:p.Thr166=
ENST00000676906.1:c.39T>A	ENSP00000503122.1:p.Thr13=
ENST00000677477.1:n.1724T>A
ENST00000678029.1:c.498T>A	ENSP00000503887.1:p.Thr166=
ENST00000678745.1:c.498T>A	ENSP00000503632.1:p.Thr166=
ENST00000679094.1:c.498T>A	ENSP00000504295.1:p.Thr166=
ENST00000679240.1:n.896T>A
ENST00000260361.8:c.498T>A	ENSP00000260361.4:p.Thr166=
ENST00000558719.1:c.498T>A	ENSP00000454083.1:p.Thr166=
ENST00000559127.5:c.498T>A	ENSP00000453027.1:p.Thr166=
ENST00000560978.1:c.498T>A	ENSP00000453944.1:p.Thr166=
NM_016013.3:c.498T>A	NP_057097.2:p.Thr166=
NR_045620.1:n.896T>A
XM_006720555.1:c.498T>A	XP_006720618.1:p.Thr166=
XM_011521658.1:c.498T>A	XP_011519960.1:p.Thr166=
XM_011521659.1:c.498T>A	XP_011519961.1:p.Thr166=
XM_006720555.3:c.498T>A	XP_006720618.1:p.Thr166=
XM_011521659.3:c.498T>A	XP_011519961.1:p.Thr166=
XM_024449945.1:c.498T>A	XP_024305713.1:p.Thr166=
NM_016013.4:c.498T>A MANE Select	NP_057097.2:p.Thr166=
NR_045620.2:n.932T>A