Canonical Allele Identifier: CA412942141

Gene: WDR45

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49075208T>A , CM000685.2:g.49075208T>A	GRCh38
NC_000023.10:g.48932867T>A , CM000685.1:g.48932867T>A	GRCh37
NC_000023.9:g.48819811T>A	NCBI36
NG_033004.1:g.30193A>T
NG_033004.2:g.30963A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001029896.2:c.901A>T MANE Select	NP_001025067.1:p.Thr301Ser
ENST00000376372.9:c.901A>T MANE Select	ENSP00000365551.3:p.Thr301Ser
NM_001029896.1:c.901A>T	NP_001025067.1:p.Thr301Ser
NM_007075.3:c.904A>T	NP_009006.2:p.Thr302Ser
NM_007075.4:c.904A>T	NP_009006.2:p.Thr302Ser
ENST00000322995.13:c.934A>T	ENSP00000365543.5:p.Thr312Ser
ENST00000356463.7:c.904A>T	ENSP00000348848.3:p.Thr302Ser
ENST00000367375.8:c.680A>T
ENST00000376358.4:c.521+156A>T	ENSP00000365536.3:n.521+156A>T
ENST00000376368.7:c.904A>T	ENSP00000365546.2:p.Thr302Ser
ENST00000376372.8:c.901A>T	ENSP00000365551.3:p.Thr301Ser
ENST00000396681.9:c.784A>T	ENSP00000379913.5:p.Thr262Ser
ENST00000433252.7:n.557A>T
ENST00000465806.6:n.2058A>T
ENST00000473974.5:c.726-296A>T	ENSP00000417211.1:n.726-296A>T
ENST00000475977.2:c.323+156A>T	ENSP00000417754.2:n.323+156A>T
ENST00000485908.6:c.796A>T	ENSP00000419897.1:p.Thr266Ser
ENST00000486337.6:c.89A>T
ENST00000634559.1:c.688A>T	ENSP00000488986.1:p.Thr230Ser
ENST00000634838.1:c.859A>T	ENSP00000489268.1:p.Thr287Ser
ENST00000634852.1:n.598A>T
ENST00000634944.1:c.901A>T	ENSP00000488972.1:p.Thr301Ser
ENST00000635003.1:c.700A>T	ENSP00000489080.1:p.Thr234Ser