Canonical Allele Identifier: CA2670361385
Gene: WDR19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39273036_39273043dup , CM000666.2:g.39273036_39273043dup GRCh38
NC_000004.11:g.39274656_39274663dup , CM000666.1:g.39274656_39274663dup GRCh37
NC_000004.10:g.38951051_38951058dup NCBI36
NG_031813.1:g.95633_95640dup

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3540_3547dup MANE Select ENSP00000382717.3:p.Ile1183ThrfsTer15
ENST00000399820.7:c.3540_3547dup ENSP00000382717.3:p.Ile1183ThrfsTer15
ENST00000506869.5:c.*3121_*3128dup ENSP00000424319.1:n.*3121_*3128dup
ENST00000512095.5:n.2538_2545dup
ENST00000512534.5:n.105_112dup
NM_025132.3:c.3540_3547dup NP_079408.3:p.Ile1183ThrfsTer15
XM_011513724.1:c.3552_3559dup XP_011512026.1:p.Ile1187ThrfsTer15
XM_011513725.1:c.3486_3493dup XP_011512027.1:p.Ile1165ThrfsTer15
XM_011513726.1:c.3072_3079dup XP_011512028.1:p.Ile1027ThrfsTer15
XM_011513727.1:c.3072_3079dup XP_011512029.1:p.Ile1027ThrfsTer15
XM_011513728.1:c.3060_3067dup XP_011512030.1:p.Ile1023ThrfsTer15
XR_925155.1:n.3616_3623dup
NM_001317924.1:c.3060_3067dup NP_001304853.1:p.Ile1023ThrfsTer15
XM_011513725.2:c.3486_3493dup XP_011512027.1:p.Ile1165ThrfsTer15
XM_011513726.3:c.3072_3079dup XP_011512028.1:p.Ile1027ThrfsTer15
XM_017008501.1:c.3060_3067dup XP_016863990.1:p.Ile1023ThrfsTer15
XR_001741306.1:n.3616_3623dup
XR_001741307.1:n.3604_3611dup
XR_001741308.1:n.3616_3623dup
XR_001741309.1:n.3604_3611dup
XR_001741310.1:n.3604_3611dup
XR_001741311.2:n.3453_3460dup
NM_025132.4:c.3540_3547dup MANE Select NP_079408.3:p.Ile1183ThrfsTer15
NM_001317924.2:c.3060_3067dup NP_001304853.1:p.Ile1023ThrfsTer15