Canonical Allele Identifier: CA1452058474
Gene: WDR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39277021A= , CM000666.2:g.39277021A= GRCh38
NC_000004.11:g.39278641A= , CM000666.1:g.39278641A= GRCh37
NC_000004.10:g.38955036A= NCBI36
NG_031813.1:g.99618A=

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3718A= MANE Select ENSP00000382717.3:p.Arg1240=
ENST00000399820.7:c.3718A= ENSP00000382717.3:p.Arg1240=
ENST00000503733.1:n.58A=
ENST00000506869.5:c.*3299A= ENSP00000424319.1:n.*3299A=
ENST00000512534.5:n.2029A=
ENST00000512588.5:n.60A=
NM_025132.3:c.3718A= NP_079408.3:p.Arg1240=
XM_011513724.1:c.3730A= XP_011512026.1:p.Arg1244=
XM_011513725.1:c.3664A= XP_011512027.1:p.Arg1222=
XM_011513726.1:c.3250A= XP_011512028.1:p.Arg1084=
XM_011513727.1:c.3250A= XP_011512029.1:p.Arg1084=
XM_011513728.1:c.3238A= XP_011512030.1:p.Arg1080=
XR_925155.1:n.5428A=
NM_001317924.1:c.3238A= NP_001304853.1:p.Arg1080=
XM_011513725.2:c.3664A= XP_011512027.1:p.Arg1222=
XM_011513726.3:c.3250A= XP_011512028.1:p.Arg1084=
XM_017008501.1:c.3238A= XP_016863990.1:p.Arg1080=
XR_001741306.1:n.3995A=
XR_001741307.1:n.3983A=
XR_001741308.1:n.5629A=
XR_001741309.1:n.5416A=
XR_001741310.1:n.5617A=
XR_001741311.2:n.5265A=
NM_025132.4:c.3718A= MANE Select NP_079408.3:p.Arg1240=
NM_001317924.2:c.3238A= NP_001304853.1:p.Arg1080=