Canonical Allele Identifier: CA412943294

Gene: WDR45

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49075543A>T , CM000685.2:g.49075543A>T	GRCh38
NC_000023.10:g.48933202A>T , CM000685.1:g.48933202A>T	GRCh37
NC_000023.9:g.48820146A>T	NCBI36
NG_033004.1:g.29858T>A
NG_033004.2:g.30628T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001029896.2:c.725+2T>A MANE Select	NP_001025067.1:n.725+2T>A
ENST00000376372.9:c.725+2T>A MANE Select	ENSP00000365551.3:n.725+2T>A
NM_001029896.1:c.725+2T>A	NP_001025067.1:n.725+2T>A
NM_007075.3:c.728+2T>A	NP_009006.2:n.728+2T>A
NM_007075.4:c.728+2T>A	NP_009006.2:n.728+2T>A
ENST00000322995.13:c.758+2T>A	ENSP00000365543.5:n.758+2T>A
ENST00000356463.7:c.728+2T>A	ENSP00000348848.3:n.728+2T>A
ENST00000367375.8:c.504+2T>A
ENST00000376358.4:c.419+2T>A	ENSP00000365536.3:n.419+2T>A
ENST00000376368.7:c.728+2T>A	ENSP00000365546.2:n.728+2T>A
ENST00000376372.8:c.725+2T>A	ENSP00000365551.3:n.725+2T>A
ENST00000396681.9:c.620+2T>A	ENSP00000379913.5:n.620+2T>A
ENST00000433252.7:n.299+2T>A
ENST00000465806.6:n.1882+2T>A
ENST00000473974.5:c.725+2T>A	ENSP00000417211.1:n.725+2T>A
ENST00000475880.6:c.623+2T>A	ENSP00000418919.2:n.623+2T>A
ENST00000475977.2:c.221+2T>A	ENSP00000417754.2:n.221+2T>A
ENST00000480412.2:n.330+2T>A
ENST00000485908.6:c.620+2T>A	ENSP00000419897.1:n.620+2T>A
ENST00000634559.1:c.524+2T>A	ENSP00000488986.1:n.524+2T>A
ENST00000634736.1:c.419+2T>A	ENSP00000489561.1:n.419+2T>A
ENST00000634838.1:c.725+2T>A	ENSP00000489268.1:n.725+2T>A
ENST00000634852.1:n.422+2T>A
ENST00000634944.1:c.725+2T>A	ENSP00000488972.1:n.725+2T>A
ENST00000635003.1:c.524+2T>A	ENSP00000489080.1:n.524+2T>A
ENST00000635344.1:c.*376+2T>A	ENSP00000489553.1:n.*376+2T>A
ENST00000635666.1:c.653+2T>A	ENSP00000489128.1:n.653+2T>A