Canonical Allele Identifier: CA1452058478
Gene: WDR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39277024C= , CM000666.2:g.39277024C= GRCh38
NC_000004.11:g.39278644C= , CM000666.1:g.39278644C= GRCh37
NC_000004.10:g.38955039C= NCBI36
NG_031813.1:g.99621C=

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3721C= MANE Select ENSP00000382717.3:p.Pro1241=
ENST00000399820.7:c.3721C= ENSP00000382717.3:p.Pro1241=
ENST00000503733.1:n.61C=
ENST00000506869.5:c.*3302C= ENSP00000424319.1:n.*3302C=
ENST00000512534.5:n.2032C=
ENST00000512588.5:n.63C=
NM_025132.3:c.3721C= NP_079408.3:p.Pro1241=
XM_011513724.1:c.3733C= XP_011512026.1:p.Pro1245=
XM_011513725.1:c.3667C= XP_011512027.1:p.Pro1223=
XM_011513726.1:c.3253C= XP_011512028.1:p.Pro1085=
XM_011513727.1:c.3253C= XP_011512029.1:p.Pro1085=
XM_011513728.1:c.3241C= XP_011512030.1:p.Pro1081=
XR_925155.1:n.5431C=
NM_001317924.1:c.3241C= NP_001304853.1:p.Pro1081=
XM_011513725.2:c.3667C= XP_011512027.1:p.Pro1223=
XM_011513726.3:c.3253C= XP_011512028.1:p.Pro1085=
XM_017008501.1:c.3241C= XP_016863990.1:p.Pro1081=
XR_001741306.1:n.3998C=
XR_001741307.1:n.3986C=
XR_001741308.1:n.5632C=
XR_001741309.1:n.5419C=
XR_001741310.1:n.5620C=
XR_001741311.2:n.5268C=
NM_025132.4:c.3721C= MANE Select NP_079408.3:p.Pro1241=
NM_001317924.2:c.3241C= NP_001304853.1:p.Pro1081=