Canonical Allele Identifier: CA391810056

Gene: NDUFAF1

Linked Data

• MyVariant Identifiers: chr15:g.41688818C>G (hg19) ; chr15:g.41396620C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41396620C>G , CM000677.2:g.41396620C>G	GRCh38
NC_000015.9:g.41688818C>G , CM000677.1:g.41688818C>G	GRCh37
NC_000015.8:g.39476110C>G	NCBI36
NG_031924.1:g.10841G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260361.9:c.440G>C MANE Select	ENSP00000260361.4:p.Arg147Thr
ENST00000558719.2:c.440G>C	ENSP00000454083.2:p.Arg147Thr
ENST00000560978.2:c.440G>C	ENSP00000453944.2:p.Arg147Thr
ENST00000676533.1:c.440G>C	ENSP00000504040.1:p.Arg147Thr
ENST00000676906.1:c.-20G>C	ENSP00000503122.1:n.-20G>C
ENST00000677477.1:n.1666G>C
ENST00000678029.1:c.440G>C	ENSP00000503887.1:p.Arg147Thr
ENST00000678745.1:c.440G>C	ENSP00000503632.1:p.Arg147Thr
ENST00000679094.1:c.440G>C	ENSP00000504295.1:p.Arg147Thr
ENST00000679240.1:n.838G>C
ENST00000260361.8:c.440G>C	ENSP00000260361.4:p.Arg147Thr
ENST00000558719.1:c.440G>C	ENSP00000454083.1:p.Arg147Thr
ENST00000559127.5:c.440G>C	ENSP00000453027.1:p.Arg147Thr
ENST00000560978.1:c.440G>C	ENSP00000453944.1:p.Arg147Thr
NM_016013.3:c.440G>C	NP_057097.2:p.Arg147Thr
NR_045620.1:n.838G>C
XM_006720555.1:c.440G>C	XP_006720618.1:p.Arg147Thr
XM_011521658.1:c.440G>C	XP_011519960.1:p.Arg147Thr
XM_011521659.1:c.440G>C	XP_011519961.1:p.Arg147Thr
XM_006720555.3:c.440G>C	XP_006720618.1:p.Arg147Thr
XM_011521659.3:c.440G>C	XP_011519961.1:p.Arg147Thr
XM_024449945.1:c.440G>C	XP_024305713.1:p.Arg147Thr
NM_016013.4:c.440G>C MANE Select	NP_057097.2:p.Arg147Thr
NR_045620.2:n.874G>C