Canonical Allele Identifier: CA324363
Gene: NDUFB9 HGNC NCBI
TATDN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.124539209C>T , CM000670.2:g.124539209C>T GRCh38
NC_000008.10:g.125551450C>T , CM000670.1:g.125551450C>T GRCh37
NC_000008.9:g.125620631C>T NCBI36
NG_042266.1:g.5108C>T

Transcript Alleles

HGVS Amino-acid Change
NM_005005.3:c.23C>T (NDUFB9) MANE Select NP_004996.1:p.Pro8Leu
ENST00000276689.8:c.23C>T (NDUFB9) MANE Select ENSP00000276689.3:p.Pro8Leu
NM_001278645.1:c.-111C>T (NDUFB9) NP_001265574.1:n.-111C>T
NM_001278645.2:c.-111C>T (NDUFB9) NP_001265574.1:n.-111C>T
NM_001278646.1:c.-105C>T (NDUFB9) NP_001265575.1:n.-105C>T
NM_001278646.2:c.-105C>T (NDUFB9) NP_001265575.1:n.-105C>T
NM_001311168.1:c.23C>T (NDUFB9) NP_001298097.1:p.Pro8Leu
NM_001311168.2:c.23C>T (NDUFB9) NP_001298097.1:p.Pro8Leu
NM_005005.2:c.23C>T (NDUFB9) NP_004996.1:p.Pro8Leu
ENST00000276689.7:c.23C>T (NDUFB9) ENSP00000276689.3:p.Pro8Leu
ENST00000517367.1:c.23C>T (NDUFB9) ENSP00000430322.1:p.Pro8Leu
ENST00000518008.5:c.23C>T (NDUFB9) ENSP00000428282.1:p.Pro8Leu
ENST00000522532.5:c.23C>T (NDUFB9) ENSP00000431115.1:p.Pro8Leu
ENST00000522532.6:c.23C>T (NDUFB9) ENSP00000431115.1:p.Pro8Leu
ENST00000523152.3:c.-163G>A (TATDN1) ENSP00000427807.1:n.-163G>A
ENST00000524241.2:n.48C>T (NDUFB9)
ENST00000606244.2:c.23C>T (NDUFB9) ENSP00000497750.1:p.Pro8Leu
ENST00000676713.1:c.23C>T (NDUFB9) ENSP00000504795.1:p.Pro8Leu
ENST00000677021.1:c.23C>T (NDUFB9) ENSP00000504235.1:p.Pro8Leu
ENST00000677782.1:n.42C>T (NDUFB9)
ENST00000677822.1:c.23C>T (NDUFB9) ENSP00000504813.1:p.Pro8Leu
ENST00000677950.1:c.23C>T (NDUFB9) ENSP00000504071.1:p.Pro8Leu
XM_024447293.1:c.-163G>A (TATDN1) XP_024303061.1:n.-163G>A