Canonical Allele Identifier: CA462752941

Gene: NDUFB9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.124549766G>A , CM000670.2:g.124549766G>A	GRCh38
NC_000008.10:g.125562007G>A , CM000670.1:g.125562007G>A	GRCh37
NC_000008.9:g.125631188G>A	NCBI36
NG_042266.1:g.15665G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005005.3:c.414G>A MANE Select	NP_004996.1:p.Lys138=
ENST00000276689.8:c.414G>A MANE Select	ENSP00000276689.3:p.Lys138=
NM_001278645.1:c.246G>A	NP_001265574.1:p.Lys82=
NM_001278645.2:c.246G>A	NP_001265574.1:p.Lys82=
NM_001278646.1:c.285G>A	NP_001265575.1:p.Lys95=
NM_001278646.2:c.285G>A	NP_001265575.1:p.Lys95=
NM_001311168.1:c.381G>A	NP_001298097.1:p.Lys127=
NM_001311168.2:c.381G>A	NP_001298097.1:p.Lys127=
NM_005005.2:c.414G>A	NP_004996.1:p.Lys138=
ENST00000276689.7:c.414G>A	ENSP00000276689.3:p.Lys138=
ENST00000517367.1:c.381G>A	ENSP00000430322.1:p.Lys127=
ENST00000518657.5:n.460G>A
ENST00000518657.6:n.1494G>A
ENST00000522532.5:c.408+2653G>A	ENSP00000431115.1:n.408+2653G>A
ENST00000522532.6:c.408+2653G>A	ENSP00000431115.1:n.408+2653G>A
ENST00000524241.1:n.442G>A
ENST00000524241.2:n.4159G>A
ENST00000606244.2:c.408+2653G>A	ENSP00000497750.1:n.408+2653G>A
ENST00000676713.1:c.*262+2653G>A	ENSP00000504795.1:n.*262+2653G>A
ENST00000677021.1:c.414G>A	ENSP00000504235.1:p.Lys138=
ENST00000677782.1:n.3080G>A
ENST00000677822.1:c.414G>A	ENSP00000504813.1:p.Lys138=
ENST00000677950.1:c.*268G>A	ENSP00000504071.1:n.*268G>A
ENST00000678753.1:n.117G>A
ENST00000678801.1:n.150+2653G>A