Canonical Allele Identifier: CA3024550477
Community Standard Title: NM_145294.5(WDR90):c.4311+505A>C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.663349A>C , CM000678.2:g.663349A>C GRCh38
NC_000016.9:g.713349A>C , CM000678.1:g.713349A>C GRCh37
NC_000016.8:g.653350A>C NCBI36
NG_031824.1:g.267A>C

Transcript Alleles

HGVS Amino-acid Change
NM_145294.5:c.4311+505A>C (WDR90) MANE Select NP_660337.3:n.4311+505A>C
ENST00000293879.9:c.4311+505A>C (WDR90) MANE Select ENSP00000293879.4:n.4311+505A>C
NM_145294.4:c.4311+505A>C (WDR90) NP_660337.3:n.4311+505A>C
ENST00000293879.8:c.4311+505A>C (WDR90) ENSP00000293879.4:n.4311+505A>C
ENST00000546516.5:n.3509A>C (WDR90)
ENST00000547407.5:n.2671+285A>C (WDR90)
ENST00000547543.5:n.210A>C (WDR90)
ENST00000548603.1:n.434A>C (WDR90)
ENST00000549024.5:n.1081+505A>C (WDR90)
ENST00000549091.5:c.4317+505A>C (WDR90) ENSP00000448122.1:n.4317+505A>C
ENST00000552683.5:n.2253A>C (WDR90)
ENST00000552728.5:c.1956+1018A>C (WDR90) ENSP00000448603.1:n.1956+1018A>C
ENST00000620831.4:c.-50+20046A>C (MSLN) ENSP00000482893.1:n.-50+20046A>C
XM_005255160.1:c.4320+505A>C (WDR90) XP_005255217.1:n.4320+505A>C
XM_011522405.1:c.4335+505A>C (WDR90) XP_011520707.1:n.4335+505A>C
XM_011522406.1:c.4332+505A>C (WDR90) XP_011520708.1:n.4332+505A>C
XM_011522407.1:c.4329+505A>C (WDR90) XP_011520709.1:n.4329+505A>C
XM_011522408.1:c.4305+505A>C (WDR90) XP_011520710.1:n.4305+505A>C
XM_011522409.1:c.4296+505A>C (WDR90) XP_011520711.1:n.4296+505A>C
XM_011522410.1:c.4119+505A>C (WDR90) XP_011520712.1:n.4119+505A>C
XM_011522411.1:c.4335+505A>C (WDR90) XP_011520713.1:n.4335+505A>C
XM_011522412.1:c.4163+1018A>C (WDR90) XP_011520714.1:n.4163+1018A>C
XM_017023023.1:c.4581+505A>C (WDR90) XP_016878512.1:n.4581+505A>C
XM_017023024.1:c.1920+505A>C (WDR90) XP_016878513.1:n.1920+505A>C
XR_932796.1:n.4894A>C (WDR90)
XR_932797.1:n.4894A>C (WDR90)
XR_932798.1:n.4594A>C (WDR90)
XR_932800.1:n.4285+505A>C (WDR90)
XR_932801.1:n.4270+505A>C (WDR90)
XR_932802.1:n.4098+1018A>C (WDR90)