Canonical Allele Identifier: CA7106499

Gene: RBM23

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22902276C>A , CM000676.2:g.22902276C>A	GRCh38
NC_000014.8:g.23371485C>A , CM000676.1:g.23371485C>A	GRCh37
NC_000014.7:g.22441325C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359890.8:c.1037G>T MANE Select	ENSP00000352956.3:p.Gly346Val
ENST00000346528.9:c.935G>T	ENSP00000339220.5:p.Gly312Val
ENST00000359890.7:c.1037G>T	ENSP00000352956.3:p.Gly346Val
ENST00000399922.6:c.989G>T	ENSP00000382806.2:p.Gly330Val
ENST00000542016.6:c.527G>T	ENSP00000438504.2:p.Gly176Val
ENST00000553884.5:c.360G>T
ENST00000555209.5:c.287G>T	ENSP00000452602.1:p.Gly96Val
ENST00000556838.5:n.157G>T
ENST00000557127.1:n.197G>T
ENST00000557667.5:n.2993G>T
NM_001077351.1:c.1037G>T	NP_001070819.1:p.Gly346Val
NM_001077352.1:c.935G>T	NP_001070820.1:p.Gly312Val
NM_001308044.1:c.527G>T	NP_001294973.1:p.Gly176Val
NM_018107.4:c.989G>T	NP_060577.3:p.Gly330Val
XM_011536890.1:c.1169G>T	XP_011535192.1:p.Gly390Val
XM_011536891.1:c.1169G>T	XP_011535193.1:p.Gly390Val
XM_011536892.1:c.1121G>T	XP_011535194.1:p.Gly374Val
XM_011536893.1:c.1121G>T	XP_011535195.1:p.Gly374Val
XM_011536894.1:c.1115G>T	XP_011535196.1:p.Gly372Val
XM_011536895.1:c.1067G>T	XP_011535197.1:p.Gly356Val
XM_011536896.1:c.1067G>T	XP_011535198.1:p.Gly356Val
XM_011536897.1:c.1043G>T	XP_011535199.1:p.Gly348Val
XM_011536898.1:c.1037G>T	XP_011535200.1:p.Gly346Val
XM_011536899.1:c.989G>T	XP_011535201.1:p.Gly330Val
XM_011536900.1:c.983G>T	XP_011535202.1:p.Gly328Val
XM_011536902.1:c.527G>T	XP_011535204.1:p.Gly176Val
XM_011536903.1:c.527G>T	XP_011535205.1:p.Gly176Val
XM_011536904.1:c.527G>T	XP_011535206.1:p.Gly176Val
XM_011536905.1:c.527G>T	XP_011535207.1:p.Gly176Val
XM_011536906.1:c.527G>T	XP_011535208.1:p.Gly176Val
NM_001352762.1:c.527G>T	NP_001339691.1:p.Gly176Val
NM_001352763.1:c.1037G>T	NP_001339692.1:p.Gly346Val
NM_001352764.1:c.1169G>T	NP_001339693.1:p.Gly390Val
NM_001352765.1:c.989G>T	NP_001339694.1:p.Gly330Val
NM_001352766.1:c.1037G>T	NP_001339695.1:p.Gly346Val
XM_011536892.2:c.1121G>T	XP_011535194.1:p.Gly374Val
XM_011536893.3:c.1121G>T	XP_011535195.1:p.Gly374Val
XM_011536894.2:c.1115G>T	XP_011535196.1:p.Gly372Val
XM_011536895.3:c.1067G>T	XP_011535197.1:p.Gly356Val
XM_011536896.3:c.1067G>T	XP_011535198.1:p.Gly356Val
XM_011536897.2:c.1043G>T	XP_011535199.1:p.Gly348Val
XM_011536900.2:c.983G>T	XP_011535202.1:p.Gly328Val
XM_017021398.2:c.1121G>T	XP_016876887.1:p.Gly374Val
XM_017021399.2:c.1067G>T	XP_016876888.1:p.Gly356Val
XM_017021400.2:c.1043G>T	XP_016876889.1:p.Gly348Val
XM_017021401.2:c.1037G>T	XP_016876890.1:p.Gly346Val
XM_017021402.2:c.1037G>T	XP_016876891.1:p.Gly346Val
XM_017021403.2:c.989G>T	XP_016876892.1:p.Gly330Val
XM_017021404.1:c.989G>T	XP_016876893.1:p.Gly330Val
XM_017021405.2:c.983G>T	XP_016876894.1:p.Gly328Val
XM_017021406.1:c.1091G>T	XP_016876895.1:p.Gly364Val
XM_017021408.1:c.935G>T	XP_016876897.1:p.Gly312Val
XM_017021409.1:c.1037G>T	XP_016876898.1:p.Gly346Val
XM_017021410.1:c.935G>T	XP_016876899.1:p.Gly312Val
XM_017021411.1:c.989G>T	XP_016876900.1:p.Gly330Val
XM_017021414.1:c.527G>T	XP_016876903.1:p.Gly176Val
XM_017021415.1:c.527G>T	XP_016876904.1:p.Gly176Val
XM_017021416.1:c.527G>T	XP_016876905.1:p.Gly176Val
XM_017021417.1:c.527G>T	XP_016876906.1:p.Gly176Val
XM_017021418.1:c.527G>T	XP_016876907.1:p.Gly176Val
XM_017021419.1:c.527G>T	XP_016876908.1:p.Gly176Val
XM_017021420.1:c.527G>T	XP_016876909.1:p.Gly176Val
XM_024449640.1:c.1169G>T	XP_024305408.1:p.Gly390Val
XM_024449641.1:c.1115G>T	XP_024305409.1:p.Gly372Val
XM_024449642.1:c.1070G>T	XP_024305410.1:p.Gly357Val
XM_024449643.1:c.989G>T	XP_024305411.1:p.Gly330Val
XM_024449645.1:c.629G>T	XP_024305413.1:p.Gly210Val
XM_024449646.1:c.629G>T	XP_024305414.1:p.Gly210Val
NM_001077351.2:c.1037G>T MANE Select	NP_001070819.1:p.Gly346Val
NM_001077352.2:c.935G>T	NP_001070820.1:p.Gly312Val
NM_001308044.2:c.527G>T	NP_001294973.1:p.Gly176Val
NM_001352762.2:c.527G>T	NP_001339691.1:p.Gly176Val
NM_001352763.2:c.1037G>T	NP_001339692.1:p.Gly346Val
NM_001352764.2:c.1169G>T	NP_001339693.1:p.Gly390Val
NM_001352765.2:c.989G>T	NP_001339694.1:p.Gly330Val
NM_001352766.2:c.1037G>T	NP_001339695.1:p.Gly346Val
NM_018107.5:c.989G>T	NP_060577.3:p.Gly330Val