Canonical Allele Identifier: CA2580588830

Gene: WDR1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.10103046A>T , CM000666.2:g.10103046A>T	GRCh38
NC_000004.11:g.10104670A>T , CM000666.1:g.10104670A>T	GRCh37
NC_000004.10:g.9713768A>T	NCBI36
NG_027876.1:g.18904T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264785.12:c.-591+850T>A	ENSP00000514597.1:n.-591+850T>A
ENST00000502702.6:c.138+13067T>A	ENSP00000426725.1:n.138+13067T>A
ENST00000699786.1:c.241+850T>A	ENSP00000514592.1:n.241+850T>A
ENST00000699787.1:c.229+850T>A	ENSP00000514593.1:n.229+850T>A
ENST00000699788.1:c.138+13067T>A	ENSP00000514594.1:n.138+13067T>A
ENST00000699790.1:c.138+13067T>A	ENSP00000514595.1:n.138+13067T>A
ENST00000699794.1:c.229+850T>A	ENSP00000514596.1:n.229+850T>A
ENST00000699795.1:c.139-3907T>A	ENSP00000514598.1:n.139-3907T>A
ENST00000699796.1:c.229+850T>A	ENSP00000514599.1:n.229+850T>A
ENST00000699797.1:c.229+850T>A	ENSP00000514600.1:n.229+850T>A
ENST00000699798.1:c.229+850T>A	ENSP00000514601.1:n.229+850T>A
ENST00000699799.1:c.229+850T>A	ENSP00000514602.1:n.229+850T>A
ENST00000499869.7:c.229+850T>A MANE Select	ENSP00000427687.1:n.229+850T>A
ENST00000264785.11:n.219+850T>A
ENST00000382451.6:c.138+13067T>A	ENSP00000371889.2:n.138+13067T>A
ENST00000382452.6:c.229+850T>A	ENSP00000371890.2:n.229+850T>A
ENST00000499869.6:c.229+850T>A	ENSP00000427687.1:n.229+850T>A
ENST00000502702.5:c.138+13067T>A	ENSP00000426725.1:n.138+13067T>A
ENST00000505851.5:n.387+850T>A
ENST00000508079.1:c.241+850T>A	ENSP00000425481.1:n.241+850T>A
ENST00000514319.5:n.523+850T>A
ENST00000515018.1:n.124+850T>A
NM_005112.4:c.138+13067T>A	NP_005103.2:n.138+13067T>A
NM_017491.3:c.229+850T>A	NP_059830.1:n.229+850T>A
NM_017491.4:c.229+850T>A	NP_059830.1:n.229+850T>A
XM_017008880.2:c.229+850T>A	XP_016864369.1:n.229+850T>A
NM_017491.5:c.229+850T>A MANE Select	NP_059830.1:n.229+850T>A
NM_005112.5:c.138+13067T>A	NP_005103.2:n.138+13067T>A