Canonical Allele Identifier: CA7013313
Community Standard Title: NM_001366735.2(RBM26):c.2911G>C (p.Glu971Gln)
Gene: RBM26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.79322372C>G , CM000675.2:g.79322372C>G GRCh38
NC_000013.10:g.79896507C>G , CM000675.1:g.79896507C>G GRCh37
NC_000013.9:g.78794508C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001366735.2:c.2911G>C MANE Select NP_001353664.1:p.Glu971Gln
ENST00000438737.3:c.2911G>C MANE Select ENSP00000387531.2:p.Glu971Gln
NM_001286631.1:c.2917G>C NP_001273560.1:p.Glu973Gln
NM_001286631.2:c.2917G>C NP_001273560.1:p.Glu973Gln
NM_001286632.1:c.2839G>C NP_001273561.1:p.Glu947Gln
NM_001286632.2:c.2839G>C NP_001273561.1:p.Glu947Gln
NM_001366735.1:c.2911G>C NP_001353664.1:p.Glu971Gln
NM_022118.4:c.2830G>C NP_071401.3:p.Glu944Gln
NM_022118.5:c.2830G>C NP_071401.3:p.Glu944Gln
ENST00000267229.11:c.2830G>C ENSP00000267229.7:p.Glu944Gln
ENST00000438724.5:c.2839G>C ENSP00000390222.1:p.Glu947Gln
ENST00000438737.2:c.2911G>C ENSP00000387531.2:p.Glu971Gln
ENST00000449987.6:c.469G>C ENSP00000401474.2:p.Glu157Gln
ENST00000622611.4:c.2917G>C ENSP00000483408.1:p.Glu973Gln
XM_005266491.3:c.2956G>C XP_005266548.1:p.Glu986Gln
XM_005266491.5:c.2956G>C XP_005266548.1:p.Glu986Gln
XM_005266497.1:c.2956G>C XP_005266554.1:p.Glu986Gln
XM_005266497.2:c.2956G>C XP_005266554.1:p.Glu986Gln
XM_006719857.1:c.2956G>C XP_006719920.1:p.Glu986Gln
XM_006719857.2:c.2956G>C XP_006719920.1:p.Glu986Gln
XM_011535179.1:c.2956G>C XP_011533481.1:p.Glu986Gln
XM_011535179.2:c.2956G>C XP_011533481.1:p.Glu986Gln
XM_011535180.1:c.2956G>C XP_011533482.1:p.Glu986Gln
XM_011535180.3:c.2956G>C XP_011533482.1:p.Glu986Gln
XM_011535181.1:c.2947G>C XP_011533483.1:p.Glu983Gln
XM_011535181.2:c.2947G>C XP_011533483.1:p.Glu983Gln
XM_011535182.1:c.2941G>C XP_011533484.1:p.Glu981Gln
XM_011535182.2:c.2941G>C XP_011533484.1:p.Glu981Gln
XM_011535183.1:c.2947G>C XP_011533485.1:p.Glu983Gln
XM_011535183.3:c.2947G>C XP_011533485.1:p.Glu983Gln
XM_011535184.1:c.2926G>C XP_011533486.1:p.Glu976Gln
XM_011535184.2:c.2926G>C XP_011533486.1:p.Glu976Gln
XM_011535185.1:c.2926G>C XP_011533487.1:p.Glu976Gln
XM_011535185.3:c.2926G>C XP_011533487.1:p.Glu976Gln
XM_011535186.1:c.2911G>C XP_011533488.1:p.Glu971Gln
XM_011535186.3:c.2911G>C XP_011533488.1:p.Glu971Gln
XM_011535187.1:c.2917G>C XP_011533489.1:p.Glu973Gln
XM_011535187.3:c.2917G>C XP_011533489.1:p.Glu973Gln
XM_011535188.1:c.2911G>C XP_011533490.1:p.Glu971Gln
XM_011535188.3:c.2911G>C XP_011533490.1:p.Glu971Gln
XM_011535189.1:c.2884G>C XP_011533491.1:p.Glu962Gln
XM_011535189.2:c.2884G>C XP_011533491.1:p.Glu962Gln
XM_011535190.1:c.2875G>C XP_011533492.1:p.Glu959Gln
XM_011535190.2:c.2875G>C XP_011533492.1:p.Glu959Gln
XM_011535191.1:c.2875G>C XP_011533493.1:p.Glu959Gln
XM_011535191.3:c.2875G>C XP_011533493.1:p.Glu959Gln
XM_011535192.1:c.2839G>C XP_011533494.1:p.Glu947Gln
XM_011535192.3:c.2839G>C XP_011533494.1:p.Glu947Gln
XM_011535193.1:c.2830G>C XP_011533495.1:p.Glu944Gln
XM_011535193.3:c.2830G>C XP_011533495.1:p.Glu944Gln
XM_011535194.1:c.2884G>C XP_011533496.1:p.Glu962Gln
XM_011535195.1:c.2092G>C XP_011533497.1:p.Glu698Gln
XM_017020688.2:c.2956G>C XP_016876177.1:p.Glu986Gln
XM_017020689.2:c.2932G>C XP_016876178.1:p.Glu978Gln
XM_017020690.2:c.2941G>C XP_016876179.1:p.Glu981Gln
XM_017020691.2:c.2932G>C XP_016876180.1:p.Glu978Gln
XM_017020692.2:c.2902G>C XP_016876181.1:p.Glu968Gln
XM_017020693.2:c.2884G>C XP_016876182.1:p.Glu962Gln
XM_017020694.2:c.2869G>C XP_016876183.1:p.Glu957Gln
XM_017020695.2:c.2860G>C XP_016876184.1:p.Glu954Gln
XM_017020696.2:c.2869G>C XP_016876185.1:p.Glu957Gln
XM_017020697.2:c.2941G>C XP_016876186.1:p.Glu981Gln
XM_017020698.2:c.2839G>C XP_016876187.1:p.Glu947Gln
XM_017020699.2:c.2854G>C XP_016876188.1:p.Glu952Gln
XM_017020700.2:c.2830G>C XP_016876189.1:p.Glu944Gln
XM_017020701.2:c.*185G>C XP_016876190.1:n.*185G>C
XM_017020702.2:c.*185G>C XP_016876191.1:n.*185G>C
XM_017020703.2:c.*185G>C XP_016876192.1:n.*185G>C
XM_024449393.1:c.2956G>C XP_024305161.1:p.Glu986Gln