Canonical Allele Identifier: CA10588789

Gene: WDR45

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49075363C>T , CM000685.2:g.49075363C>T	GRCh38
NC_000023.10:g.48933022C>T , CM000685.1:g.48933022C>T	GRCh37
NC_000023.9:g.48819966C>T	NCBI36
NG_033004.1:g.30038G>A
NG_033004.2:g.30808G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376372.9:c.827+1G>A MANE Select	ENSP00000365551.3:n.827+1G>A
ENST00000322995.13:c.860+1G>A	ENSP00000365543.5:n.860+1G>A
ENST00000356463.7:c.830+1G>A	ENSP00000348848.3:n.830+1G>A
ENST00000367375.8:c.606+1G>A
ENST00000376358.4:c.521+1G>A	ENSP00000365536.3:n.521+1G>A
ENST00000376368.7:c.830+1G>A	ENSP00000365546.2:n.830+1G>A
ENST00000376372.8:c.827+1G>A	ENSP00000365551.3:n.827+1G>A
ENST00000396681.9:c.710+1G>A	ENSP00000379913.5:n.710+1G>A
ENST00000433252.7:n.402G>A
ENST00000465806.6:n.1984+1G>A
ENST00000473974.5:c.725+182G>A	ENSP00000417211.1:n.725+182G>A
ENST00000475977.2:c.323+1G>A	ENSP00000417754.2:n.323+1G>A
ENST00000480412.2:n.433G>A
ENST00000485908.6:c.722+1G>A	ENSP00000419897.1:n.722+1G>A
ENST00000486337.6:c.15+1G>A
ENST00000634559.1:c.614+1G>A	ENSP00000488986.1:n.614+1G>A
ENST00000634736.1:c.521+1G>A	ENSP00000489561.1:n.521+1G>A
ENST00000634838.1:c.785+1G>A	ENSP00000489268.1:n.785+1G>A
ENST00000634852.1:n.524+1G>A
ENST00000634944.1:c.827+1G>A	ENSP00000488972.1:n.827+1G>A
ENST00000635003.1:c.626+1G>A	ENSP00000489080.1:n.626+1G>A
ENST00000635666.1:c.755+1G>A	ENSP00000489128.1:n.755+1G>A
NM_001029896.1:c.827+1G>A	NP_001025067.1:n.827+1G>A
NM_007075.3:c.830+1G>A	NP_009006.2:n.830+1G>A
NM_001029896.2:c.827+1G>A MANE Select	NP_001025067.1:n.827+1G>A
NM_007075.4:c.830+1G>A	NP_009006.2:n.830+1G>A