Canonical Allele Identifier: CA4871597

Gene: NDUFB9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.124549829G>A , CM000670.2:g.124549829G>A	GRCh38
NC_000008.10:g.125562070G>A , CM000670.1:g.125562070G>A	GRCh37
NC_000008.9:g.125631251G>A	NCBI36
NG_042266.1:g.15728G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276689.8:c.477G>A MANE Select	ENSP00000276689.3:p.Lys159=
ENST00000518657.6:n.1557G>A
ENST00000522532.6:c.408+2716G>A	ENSP00000431115.1:n.408+2716G>A
ENST00000524241.2:n.4222G>A
ENST00000606244.2:c.408+2716G>A	ENSP00000497750.1:n.408+2716G>A
ENST00000676713.1:c.*262+2716G>A	ENSP00000504795.1:n.*262+2716G>A
ENST00000677021.1:c.477G>A	ENSP00000504235.1:p.Lys159=
ENST00000677782.1:n.3143G>A
ENST00000677822.1:c.477G>A	ENSP00000504813.1:p.Lys159=
ENST00000677950.1:c.*331G>A	ENSP00000504071.1:n.*331G>A
ENST00000678753.1:n.180G>A
ENST00000678801.1:n.150+2716G>A
ENST00000276689.7:c.477G>A	ENSP00000276689.3:p.Lys159=
ENST00000517367.1:c.444G>A	ENSP00000430322.1:p.Lys148=
ENST00000517830.1:n.56G>A
ENST00000518657.5:n.523G>A
ENST00000522532.5:c.408+2716G>A	ENSP00000431115.1:n.408+2716G>A
ENST00000524241.1:n.505G>A
NM_001278645.1:c.309G>A	NP_001265574.1:p.Lys103=
NM_001278646.1:c.348G>A	NP_001265575.1:p.Lys116=
NM_001311168.1:c.444G>A	NP_001298097.1:p.Lys148=
NM_005005.2:c.477G>A	NP_004996.1:p.Lys159=
NM_005005.3:c.477G>A MANE Select	NP_004996.1:p.Lys159=
NM_001278645.2:c.309G>A	NP_001265574.1:p.Lys103=
NM_001278646.2:c.348G>A	NP_001265575.1:p.Lys116=
NM_001311168.2:c.444G>A	NP_001298097.1:p.Lys148=