Canonical Allele Identifier: CA2428489958

Gene: WDR45

Linked Data

• dbSNP Id: rs2065030460

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49075357T>C , CM000685.2:g.49075357T>C	GRCh38
NC_000023.10:g.48933016T>C , CM000685.1:g.48933016T>C	GRCh37
NC_000023.9:g.48819960T>C	NCBI36
NG_033004.1:g.30044A>G
NG_033004.2:g.30814A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376372.9:c.827+7A>G MANE Select	ENSP00000365551.3:n.827+7A>G
ENST00000322995.13:c.860+7A>G	ENSP00000365543.5:n.860+7A>G
ENST00000356463.7:c.830+7A>G	ENSP00000348848.3:n.830+7A>G
ENST00000367375.8:c.606+7A>G
ENST00000376358.4:c.521+7A>G	ENSP00000365536.3:n.521+7A>G
ENST00000376368.7:c.830+7A>G	ENSP00000365546.2:n.830+7A>G
ENST00000376372.8:c.827+7A>G	ENSP00000365551.3:n.827+7A>G
ENST00000396681.9:c.710+7A>G	ENSP00000379913.5:n.710+7A>G
ENST00000433252.7:n.408A>G
ENST00000465806.6:n.1984+7A>G
ENST00000473974.5:c.725+188A>G	ENSP00000417211.1:n.725+188A>G
ENST00000475977.2:c.323+7A>G	ENSP00000417754.2:n.323+7A>G
ENST00000485908.6:c.722+7A>G	ENSP00000419897.1:n.722+7A>G
ENST00000486337.6:c.15+7A>G
ENST00000634559.1:c.614+7A>G	ENSP00000488986.1:n.614+7A>G
ENST00000634736.1:c.521+7A>G	ENSP00000489561.1:n.521+7A>G
ENST00000634838.1:c.785+7A>G	ENSP00000489268.1:n.785+7A>G
ENST00000634852.1:n.524+7A>G
ENST00000634944.1:c.827+7A>G	ENSP00000488972.1:n.827+7A>G
ENST00000635003.1:c.626+7A>G	ENSP00000489080.1:n.626+7A>G
ENST00000635666.1:c.755+7A>G	ENSP00000489128.1:n.755+7A>G
NM_001029896.1:c.827+7A>G	NP_001025067.1:n.827+7A>G
NM_007075.3:c.830+7A>G	NP_009006.2:n.830+7A>G
NM_001029896.2:c.827+7A>G MANE Select	NP_001025067.1:n.827+7A>G
NM_007075.4:c.830+7A>G	NP_009006.2:n.830+7A>G