Canonical Allele Identifier: CA10603601
Gene: WDR45 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49075420_49075421del , CM000685.2:g.49075420_49075421del GRCh38
NC_000023.10:g.48933079_48933080del , CM000685.1:g.48933079_48933080del GRCh37
NC_000023.9:g.48820023_48820024del NCBI36
NG_033004.1:g.29981_29982del
NG_033004.2:g.30751_30752del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376372.9:c.771_772del MANE Select ENSP00000365551.3:p.Asp257GlufsTer?
ENST00000322995.13:c.804_805del ENSP00000365543.5:p.Asp268GlufsTer?
ENST00000356463.7:c.774_775del ENSP00000348848.3:p.Asp258GlufsTer?
ENST00000367375.8:c.550_551del
ENST00000376358.4:c.465_466del ENSP00000365536.3:p.Asp155GlufsTer?
ENST00000376368.7:c.774_775del ENSP00000365546.2:p.Asp258GlufsTer?
ENST00000376372.8:c.771_772del ENSP00000365551.3:p.Asp257GlufsTer?
ENST00000396681.9:c.654_655del ENSP00000379913.5:p.Asp218GlufsTer?
ENST00000433252.7:n.345_346del
ENST00000465806.6:n.1928_1929del
ENST00000473974.5:c.725+125_725+126del ENSP00000417211.1:n.725+125_725+126del
ENST00000475880.6:c.669_670del ENSP00000418919.2:p.Asp223GlufsTer?
ENST00000475977.2:c.267_268del ENSP00000417754.2:p.Asp89GlufsTer23
ENST00000480412.2:n.376_377del
ENST00000485908.6:c.666_667del ENSP00000419897.1:p.Asp222GlufsTer?
ENST00000634559.1:c.558_559del ENSP00000488986.1:p.Asp186GlufsTer?
ENST00000634736.1:c.465_466del ENSP00000489561.1:p.Asp155GlufsTer?
ENST00000634838.1:c.729_730del ENSP00000489268.1:p.Asp243GlufsTer?
ENST00000634852.1:n.468_469del
ENST00000634944.1:c.771_772del ENSP00000488972.1:p.Asp257GlufsTer?
ENST00000635003.1:c.570_571del ENSP00000489080.1:p.Asp190GlufsTer?
ENST00000635344.1:c.*422_*423del ENSP00000489553.1:n.*422_*423del
ENST00000635666.1:c.699_700del ENSP00000489128.1:p.Asp233GlufsTer?
NM_001029896.1:c.771_772del NP_001025067.1:p.Asp257GlufsTer?
NM_007075.3:c.774_775del NP_009006.2:p.Asp258GlufsTer?
NM_001029896.2:c.771_772del MANE Select NP_001025067.1:p.Asp257GlufsTer?
NM_007075.4:c.774_775del NP_009006.2:p.Asp258GlufsTer?