Canonical Allele Identifier: CA7106785

Gene: RBM23

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22906294C>T , CM000676.2:g.22906294C>T	GRCh38
NC_000014.8:g.23375503C>T , CM000676.1:g.23375503C>T	GRCh37
NC_000014.7:g.22445343C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359890.8:c.302G>A MANE Select	ENSP00000352956.3:p.Arg101His
ENST00000307814.10:n.463G>A
ENST00000346528.9:c.254G>A	ENSP00000339220.5:p.Arg85His
ENST00000359890.7:c.302G>A	ENSP00000352956.3:p.Arg101His
ENST00000399922.6:c.254G>A	ENSP00000382806.2:p.Arg85His
ENST00000542016.6:c.-209G>A	ENSP00000438504.2:n.-209G>A
ENST00000553902.5:n.302G>A
ENST00000553920.5:n.337G>A
ENST00000554256.5:c.302G>A	ENSP00000452583.1:p.Arg101His
ENST00000554955.5:n.424G>A
ENST00000555209.5:c.-370G>A	ENSP00000452602.1:n.-370G>A
ENST00000555676.5:c.254G>A	ENSP00000451364.1:p.Arg85His
ENST00000555714.5:n.350G>A
ENST00000555722.5:c.-209G>A	ENSP00000450556.1:n.-209G>A
ENST00000556687.5:n.415G>A
ENST00000556984.5:n.482G>A
ENST00000557227.5:c.-155G>A	ENSP00000450423.1:n.-155G>A
ENST00000557403.5:c.-155G>A	ENSP00000452171.1:n.-155G>A
ENST00000557549.5:c.254G>A	ENSP00000450558.1:p.Arg85His
ENST00000557571.5:c.254G>A	ENSP00000452382.1:p.Arg85His
ENST00000557667.5:n.450G>A
NM_001077351.1:c.302G>A	NP_001070819.1:p.Arg101His
NM_001077352.1:c.254G>A	NP_001070820.1:p.Arg85His
NM_001308044.1:c.-209G>A	NP_001294973.1:n.-209G>A
NM_018107.4:c.254G>A	NP_060577.3:p.Arg85His
XM_011536890.1:c.434G>A	XP_011535192.1:p.Arg145His
XM_011536891.1:c.434G>A	XP_011535193.1:p.Arg145His
XM_011536892.1:c.386G>A	XP_011535194.1:p.Arg129His
XM_011536893.1:c.386G>A	XP_011535195.1:p.Arg129His
XM_011536894.1:c.434G>A	XP_011535196.1:p.Arg145His
XM_011536895.1:c.386G>A	XP_011535197.1:p.Arg129His
XM_011536896.1:c.386G>A	XP_011535198.1:p.Arg129His
XM_011536897.1:c.308G>A	XP_011535199.1:p.Arg103His
XM_011536898.1:c.302G>A	XP_011535200.1:p.Arg101His
XM_011536899.1:c.254G>A	XP_011535201.1:p.Arg85His
XM_011536900.1:c.302G>A	XP_011535202.1:p.Arg101His
XM_011536901.1:c.434G>A	XP_011535203.1:p.Arg145His
XM_011536902.1:c.-209G>A	XP_011535204.1:n.-209G>A
XM_011536903.1:c.-209G>A	XP_011535205.1:n.-209G>A
XM_011536904.1:c.-155G>A	XP_011535206.1:n.-155G>A
XM_011536905.1:c.-155G>A	XP_011535207.1:n.-155G>A
XM_011536906.1:c.-155G>A	XP_011535208.1:n.-155G>A
NM_001352762.1:c.-209G>A	NP_001339691.1:n.-209G>A
NM_001352763.1:c.302G>A	NP_001339692.1:p.Arg101His
NM_001352764.1:c.434G>A	NP_001339693.1:p.Arg145His
NM_001352765.1:c.254G>A	NP_001339694.1:p.Arg85His
NM_001352766.1:c.302G>A	NP_001339695.1:p.Arg101His
XM_011536892.2:c.386G>A	XP_011535194.1:p.Arg129His
XM_011536893.3:c.386G>A	XP_011535195.1:p.Arg129His
XM_011536894.2:c.434G>A	XP_011535196.1:p.Arg145His
XM_011536895.3:c.386G>A	XP_011535197.1:p.Arg129His
XM_011536896.3:c.386G>A	XP_011535198.1:p.Arg129His
XM_011536897.2:c.308G>A	XP_011535199.1:p.Arg103His
XM_011536900.2:c.302G>A	XP_011535202.1:p.Arg101His
XM_017021398.2:c.386G>A	XP_016876887.1:p.Arg129His
XM_017021399.2:c.386G>A	XP_016876888.1:p.Arg129His
XM_017021400.2:c.308G>A	XP_016876889.1:p.Arg103His
XM_017021401.2:c.302G>A	XP_016876890.1:p.Arg101His
XM_017021402.2:c.302G>A	XP_016876891.1:p.Arg101His
XM_017021403.2:c.254G>A	XP_016876892.1:p.Arg85His
XM_017021404.1:c.254G>A	XP_016876893.1:p.Arg85His
XM_017021405.2:c.302G>A	XP_016876894.1:p.Arg101His
XM_017021406.1:c.356G>A	XP_016876895.1:p.Arg119His
XM_017021408.1:c.254G>A	XP_016876897.1:p.Arg85His
XM_017021409.1:c.356G>A	XP_016876898.1:p.Arg119His
XM_017021410.1:c.254G>A	XP_016876899.1:p.Arg85His
XM_017021411.1:c.308G>A	XP_016876900.1:p.Arg103His
XM_017021414.1:c.-209G>A	XP_016876903.1:n.-209G>A
XM_017021415.1:c.-209G>A	XP_016876904.1:n.-209G>A
XM_017021416.1:c.-209G>A	XP_016876905.1:n.-209G>A
XM_017021417.1:c.-155G>A	XP_016876906.1:n.-155G>A
XM_017021418.1:c.-155G>A	XP_016876907.1:n.-155G>A
XM_017021419.1:c.-155G>A	XP_016876908.1:n.-155G>A
XM_017021420.1:c.-155G>A	XP_016876909.1:n.-155G>A
XM_024449640.1:c.434G>A	XP_024305408.1:p.Arg145His
XM_024449641.1:c.434G>A	XP_024305409.1:p.Arg145His
XM_024449642.1:c.254G>A	XP_024305410.1:p.Arg85His
XM_024449643.1:c.254G>A	XP_024305411.1:p.Arg85His
XM_024449644.1:c.434G>A	XP_024305412.1:p.Arg145His
XM_024449645.1:c.-794G>A	XP_024305413.1:n.-794G>A
XM_024449646.1:c.-794G>A	XP_024305414.1:n.-794G>A
NM_001077351.2:c.302G>A MANE Select	NP_001070819.1:p.Arg101His
NM_001077352.2:c.254G>A	NP_001070820.1:p.Arg85His
NM_001308044.2:c.-209G>A	NP_001294973.1:n.-209G>A
NM_001352762.2:c.-209G>A	NP_001339691.1:n.-209G>A
NM_001352763.2:c.302G>A	NP_001339692.1:p.Arg101His
NM_001352764.2:c.434G>A	NP_001339693.1:p.Arg145His
NM_001352765.2:c.254G>A	NP_001339694.1:p.Arg85His
NM_001352766.2:c.302G>A	NP_001339695.1:p.Arg101His
NM_018107.5:c.254G>A	NP_060577.3:p.Arg85His