Canonical Allele Identifier: CA10408510

Gene: WDR45

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49075896C>T , CM000685.2:g.49075896C>T	GRCh38
NC_000023.10:g.48933555C>T , CM000685.1:g.48933555C>T	GRCh37
NC_000023.9:g.48820499C>T	NCBI36
NG_033004.1:g.29505G>A
NG_033004.2:g.30275G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001029896.2:c.486G>A MANE Select	NP_001025067.1:p.Pro162=
ENST00000376372.9:c.486G>A MANE Select	ENSP00000365551.3:p.Pro162=
NM_001029896.1:c.486G>A	NP_001025067.1:p.Pro162=
NM_007075.3:c.489G>A	NP_009006.2:p.Pro163=
NM_007075.4:c.489G>A	NP_009006.2:p.Pro163=
ENST00000322995.13:c.519G>A	ENSP00000365543.5:p.Pro173=
ENST00000356463.7:c.489G>A	ENSP00000348848.3:p.Pro163=
ENST00000367375.8:c.355G>A
ENST00000376358.4:c.180G>A	ENSP00000365536.3:p.Pro60=
ENST00000376368.7:c.489G>A	ENSP00000365546.2:p.Pro163=
ENST00000376372.8:c.486G>A	ENSP00000365551.3:p.Pro162=
ENST00000396681.9:c.381G>A	ENSP00000379913.5:p.Pro127=
ENST00000419567.7:c.510G>A	ENSP00000393640.3:p.Pro170=
ENST00000423215.3:c.540G>A	ENSP00000397657.3:p.Pro180=
ENST00000433252.7:n.60G>A
ENST00000465806.6:n.1643G>A
ENST00000471338.6:c.486G>A	ENSP00000418466.2:p.Pro162=
ENST00000472654.1:n.476G>A
ENST00000473974.5:c.486G>A	ENSP00000417211.1:p.Pro162=
ENST00000474053.6:c.561G>A	ENSP00000420728.1:p.Pro187=
ENST00000475880.6:c.384G>A	ENSP00000418919.2:p.Pro128=
ENST00000476728.5:c.414G>A	ENSP00000419324.1:p.Pro138=
ENST00000485908.6:c.381G>A	ENSP00000419897.1:p.Pro127=
ENST00000634522.1:c.*137G>A	ENSP00000489330.1:n.*137G>A
ENST00000634559.1:c.285G>A	ENSP00000488986.1:p.Pro95=
ENST00000634736.1:c.180G>A	ENSP00000489561.1:p.Pro60=
ENST00000634838.1:c.486G>A	ENSP00000489268.1:p.Pro162=
ENST00000634852.1:n.183G>A
ENST00000634944.1:c.486G>A	ENSP00000488972.1:p.Pro162=
ENST00000635003.1:c.285G>A	ENSP00000489080.1:p.Pro95=
ENST00000635344.1:c.*137G>A	ENSP00000489553.1:n.*137G>A
ENST00000635666.1:c.414G>A	ENSP00000489128.1:p.Pro138=