Canonical Allele Identifier: CA7013669

Gene: RBM26

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.79358422T>C , CM000675.2:g.79358422T>C	GRCh38
NC_000013.10:g.79932557T>C , CM000675.1:g.79932557T>C	GRCh37
NC_000013.9:g.78830558T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438737.3:c.1541A>G MANE Select	ENSP00000387531.2:p.Asn514Ser
ENST00000267229.11:c.1541A>G	ENSP00000267229.7:p.Asn514Ser
ENST00000438724.5:c.1541A>G	ENSP00000390222.1:p.Asn514Ser
ENST00000438737.2:c.1541A>G	ENSP00000387531.2:p.Asn514Ser
ENST00000622611.4:c.1556A>G	ENSP00000483408.1:p.Asn519Ser
NM_001286631.1:c.1556A>G	NP_001273560.1:p.Asn519Ser
NM_001286632.1:c.1541A>G	NP_001273561.1:p.Asn514Ser
NM_022118.4:c.1541A>G	NP_071401.3:p.Asn514Ser
XM_005266491.3:c.1586A>G	XP_005266548.1:p.Asn529Ser
XM_005266497.1:c.1586A>G	XP_005266554.1:p.Asn529Ser
XM_006719857.1:c.1586A>G	XP_006719920.1:p.Asn529Ser
XM_011535179.1:c.1586A>G	XP_011533481.1:p.Asn529Ser
XM_011535180.1:c.1586A>G	XP_011533482.1:p.Asn529Ser
XM_011535181.1:c.1586A>G	XP_011533483.1:p.Asn529Ser
XM_011535182.1:c.1571A>G	XP_011533484.1:p.Asn524Ser
XM_011535183.1:c.1586A>G	XP_011533485.1:p.Asn529Ser
XM_011535184.1:c.1556A>G	XP_011533486.1:p.Asn519Ser
XM_011535185.1:c.1556A>G	XP_011533487.1:p.Asn519Ser
XM_011535186.1:c.1541A>G	XP_011533488.1:p.Asn514Ser
XM_011535187.1:c.1556A>G	XP_011533489.1:p.Asn519Ser
XM_011535188.1:c.1541A>G	XP_011533490.1:p.Asn514Ser
XM_011535189.1:c.1586A>G	XP_011533491.1:p.Asn529Ser
XM_011535190.1:c.1586A>G	XP_011533492.1:p.Asn529Ser
XM_011535191.1:c.1586A>G	XP_011533493.1:p.Asn529Ser
XM_011535192.1:c.1541A>G	XP_011533494.1:p.Asn514Ser
XM_011535193.1:c.1541A>G	XP_011533495.1:p.Asn514Ser
XM_011535194.1:c.1586A>G	XP_011533496.1:p.Asn529Ser
XM_011535195.1:c.722A>G	XP_011533497.1:p.Asn241Ser
NM_001366735.1:c.1541A>G	NP_001353664.1:p.Asn514Ser
XM_005266491.5:c.1586A>G	XP_005266548.1:p.Asn529Ser
XM_005266497.2:c.1586A>G	XP_005266554.1:p.Asn529Ser
XM_006719857.2:c.1586A>G	XP_006719920.1:p.Asn529Ser
XM_011535179.2:c.1586A>G	XP_011533481.1:p.Asn529Ser
XM_011535180.3:c.1586A>G	XP_011533482.1:p.Asn529Ser
XM_011535181.2:c.1586A>G	XP_011533483.1:p.Asn529Ser
XM_011535182.2:c.1571A>G	XP_011533484.1:p.Asn524Ser
XM_011535183.3:c.1586A>G	XP_011533485.1:p.Asn529Ser
XM_011535184.2:c.1556A>G	XP_011533486.1:p.Asn519Ser
XM_011535185.3:c.1556A>G	XP_011533487.1:p.Asn519Ser
XM_011535186.3:c.1541A>G	XP_011533488.1:p.Asn514Ser
XM_011535187.3:c.1556A>G	XP_011533489.1:p.Asn519Ser
XM_011535188.3:c.1541A>G	XP_011533490.1:p.Asn514Ser
XM_011535189.2:c.1586A>G	XP_011533491.1:p.Asn529Ser
XM_011535190.2:c.1586A>G	XP_011533492.1:p.Asn529Ser
XM_011535191.3:c.1586A>G	XP_011533493.1:p.Asn529Ser
XM_011535192.3:c.1541A>G	XP_011533494.1:p.Asn514Ser
XM_011535193.3:c.1541A>G	XP_011533495.1:p.Asn514Ser
XM_017020688.2:c.1586A>G	XP_016876177.1:p.Asn529Ser
XM_017020689.2:c.1571A>G	XP_016876178.1:p.Asn524Ser
XM_017020690.2:c.1571A>G	XP_016876179.1:p.Asn524Ser
XM_017020691.2:c.1571A>G	XP_016876180.1:p.Asn524Ser
XM_017020692.2:c.1541A>G	XP_016876181.1:p.Asn514Ser
XM_017020693.2:c.1586A>G	XP_016876182.1:p.Asn529Ser
XM_017020694.2:c.1571A>G	XP_016876183.1:p.Asn524Ser
XM_017020695.2:c.1571A>G	XP_016876184.1:p.Asn524Ser
XM_017020696.2:c.1571A>G	XP_016876185.1:p.Asn524Ser
XM_017020697.2:c.1571A>G	XP_016876186.1:p.Asn524Ser
XM_017020698.2:c.1541A>G	XP_016876187.1:p.Asn514Ser
XM_017020699.2:c.1556A>G	XP_016876188.1:p.Asn519Ser
XM_017020700.2:c.1541A>G	XP_016876189.1:p.Asn514Ser
XM_017020701.2:c.1586A>G	XP_016876190.1:p.Asn529Ser
XM_017020702.2:c.1586A>G	XP_016876191.1:p.Asn529Ser
XM_017020703.2:c.1556A>G	XP_016876192.1:p.Asn519Ser
XM_024449393.1:c.1586A>G	XP_024305161.1:p.Asn529Ser
NM_001366735.2:c.1541A>G MANE Select	NP_001353664.1:p.Asn514Ser
NM_022118.5:c.1541A>G	NP_071401.3:p.Asn514Ser
NM_001286631.2:c.1556A>G	NP_001273560.1:p.Asn519Ser
NM_001286632.2:c.1541A>G	NP_001273561.1:p.Asn514Ser