Canonical Allele Identifier: CA266786304

Gene: WDR25

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.100381627C>A , CM000676.2:g.100381627C>A	GRCh38
NC_000014.8:g.100847964C>A , CM000676.1:g.100847964C>A	GRCh37
NC_000014.7:g.99917717C>A	NCBI36
NG_053195.1:g.10218C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001161476.3:c.703C>A MANE Select	NP_001154948.1:p.Pro235Thr
ENST00000402312.8:c.703C>A MANE Select	ENSP00000385540.3:p.Pro235Thr
NM_001161476.1:c.703C>A	NP_001154948.1:p.Pro235Thr
NM_001161476.2:c.703C>A	NP_001154948.1:p.Pro235Thr
NM_001350947.1:c.703C>A	NP_001337876.1:p.Pro235Thr
NM_001350947.2:c.703C>A	NP_001337876.1:p.Pro235Thr
NM_001350948.1:c.703C>A	NP_001337877.1:p.Pro235Thr
NM_001350948.2:c.703C>A	NP_001337877.1:p.Pro235Thr
NM_001350949.1:c.-3+5123C>A	NP_001337878.1:n.-3+5123C>A
NM_001350949.2:c.-3+5123C>A	NP_001337878.1:n.-3+5123C>A
NM_001350950.1:c.48+5132C>A	NP_001337879.1:n.48+5132C>A
NM_001387351.1:c.-3+5132C>A	NP_001374280.1:n.-3+5132C>A
NM_024515.4:c.703C>A	NP_078791.3:p.Pro235Thr
NM_024515.5:c.703C>A	NP_078791.3:p.Pro235Thr
NM_024515.6:c.703C>A	NP_078791.3:p.Pro235Thr
ENST00000335290.10:c.703C>A	ENSP00000334148.6:p.Pro235Thr
ENST00000402312.7:c.703C>A	ENSP00000385540.3:p.Pro235Thr
ENST00000554175.5:c.703C>A	ENSP00000450727.1:p.Pro235Thr
ENST00000554492.5:n.205+4923C>A
ENST00000554998.5:c.703C>A	ENSP00000450661.1:p.Pro235Thr
ENST00000555775.5:n.78+5132C>A
ENST00000557710.5:c.703C>A	ENSP00000451070.1:p.Pro235Thr
XM_005268056.3:c.703C>A	XP_005268113.1:p.Pro235Thr
XM_005268057.3:c.57+5123C>A	XP_005268114.1:n.57+5123C>A
XM_005268058.3:c.48+5132C>A	XP_005268115.1:n.48+5132C>A
XM_011537150.1:c.703C>A	XP_011535452.1:p.Pro235Thr