Canonical Allele Identifier: CA2891700
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 446634
dbSNP Id: rs748656635

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39205627dup , CM000666.2:g.39205627dup GRCh38
NC_000004.11:g.39207247dup , CM000666.1:g.39207247dup GRCh37
NC_000004.10:g.38883642dup NCBI36
NG_031813.1:g.28224dup

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.781dup MANE Select ENSP00000382717.3:p.Thr261AsnfsTer13
ENST00000399820.7:c.781dup ENSP00000382717.3:p.Thr261AsnfsTer13
ENST00000503697.5:c.*249dup ENSP00000423706.1:n.*249dup
ENST00000506503.1:c.781dup ENSP00000423491.1:p.Thr261AsnfsTer13
ENST00000506869.5:c.*362dup ENSP00000424319.1:n.*362dup
ENST00000511729.5:n.41-22931dup
ENST00000512448.1:n.375dup
NM_025132.3:c.781dup NP_079408.3:p.Thr261AsnfsTer13
XM_011513724.1:c.781dup XP_011512026.1:p.Thr261AsnfsTer13
XM_011513725.1:c.715dup XP_011512027.1:p.Thr239AsnfsTer13
XM_011513726.1:c.301dup XP_011512028.1:p.Thr101AsnfsTer13
XM_011513727.1:c.301dup XP_011512029.1:p.Thr101AsnfsTer13
XM_011513728.1:c.301dup XP_011512030.1:p.Thr101AsnfsTer13
XM_011513729.1:c.781dup XP_011512031.1:p.Thr261AsnfsTer13
XR_925155.1:n.845dup
NM_001317924.1:c.301dup NP_001304853.1:p.Thr101AsnfsTer13
XM_011513725.2:c.715dup XP_011512027.1:p.Thr239AsnfsTer13
XM_011513726.3:c.301dup XP_011512028.1:p.Thr101AsnfsTer13
XM_017008501.1:c.301dup XP_016863990.1:p.Thr101AsnfsTer13
XR_001741306.1:n.845dup
XR_001741307.1:n.845dup
XR_001741308.1:n.845dup
XR_001741309.1:n.845dup
XR_001741310.1:n.845dup
XR_001741311.2:n.694dup
XR_001741312.1:n.845dup
NM_025132.4:c.781dup MANE Select NP_079408.3:p.Thr261AsnfsTer13
NM_001317924.2:c.301dup NP_001304853.1:p.Thr101AsnfsTer13