Canonical Allele Identifier: CA390976417

Gene: WDR25

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.100468021G>C , CM000676.2:g.100468021G>C	GRCh38
NC_000014.8:g.100934358G>C , CM000676.1:g.100934358G>C	GRCh37
NC_000014.7:g.100004111G>C	NCBI36
NG_053195.1:g.96612G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001161476.3:c.823G>C MANE Select	NP_001154948.1:p.Val275Leu
ENST00000402312.8:c.823G>C MANE Select	ENSP00000385540.3:p.Val275Leu
NM_001161476.1:c.823G>C	NP_001154948.1:p.Val275Leu
NM_001161476.2:c.823G>C	NP_001154948.1:p.Val275Leu
NM_001350947.1:c.823G>C	NP_001337876.1:p.Val275Leu
NM_001350947.2:c.823G>C	NP_001337876.1:p.Val275Leu
NM_001350948.1:c.823G>C	NP_001337877.1:p.Val275Leu
NM_001350948.2:c.823G>C	NP_001337877.1:p.Val275Leu
NM_001350949.1:c.73G>C	NP_001337878.1:p.Val25Leu
NM_001350949.2:c.73G>C	NP_001337878.1:p.Val25Leu
NM_001350950.1:c.49G>C	NP_001337879.1:p.Val17Leu
NM_001387351.1:c.73G>C	NP_001374280.1:p.Val25Leu
NM_024515.4:c.823G>C	NP_078791.3:p.Val275Leu
NM_024515.5:c.823G>C	NP_078791.3:p.Val275Leu
NM_024515.6:c.823G>C	NP_078791.3:p.Val275Leu
ENST00000335290.10:c.823G>C	ENSP00000334148.6:p.Val275Leu
ENST00000402312.7:c.823G>C	ENSP00000385540.3:p.Val275Leu
ENST00000542471.2:c.52G>C	ENSP00000441903.2:p.Val18Leu
ENST00000554492.5:n.206G>C
ENST00000554998.5:c.823G>C	ENSP00000450661.1:p.Val275Leu
ENST00000555775.5:n.79G>C
ENST00000557710.5:c.823-15973G>C	ENSP00000451070.1:n.823-15973G>C
XM_005268056.3:c.823G>C	XP_005268113.1:p.Val275Leu
XM_005268057.3:c.58G>C	XP_005268114.1:p.Val20Leu
XM_005268058.3:c.49G>C	XP_005268115.1:p.Val17Leu
XM_011537150.1:c.823G>C	XP_011535452.1:p.Val275Leu
XM_011537151.1:c.22G>C	XP_011535453.1:p.Val8Leu
XM_011537151.3:c.124G>C	XP_011535453.2:p.Val42Leu
XM_011537152.1:c.73G>C	XP_011535454.1:p.Val25Leu