Canonical Allele Identifier: CA1452063068
Gene: WDR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39244384T= , CM000666.2:g.39244384T= GRCh38
NC_000004.11:g.39246004T= , CM000666.1:g.39246004T= GRCh37
NC_000004.10:g.38922399T= NCBI36
NG_031813.1:g.66981T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399820.8:c.2558T= MANE Select ENSP00000382717.3:p.Met853=
ENST00000399820.7:c.2558T= ENSP00000382717.3:p.Met853=
ENST00000506869.5:c.*2139T= ENSP00000424319.1:n.*2139T=
ENST00000512095.5:n.1556T=
NM_025132.3:c.2558T= NP_079408.3:p.Met853=
XM_011513724.1:c.2570T= XP_011512026.1:p.Met857=
XM_011513725.1:c.2504T= XP_011512027.1:p.Met835=
XM_011513726.1:c.2090T= XP_011512028.1:p.Met697=
XM_011513727.1:c.2090T= XP_011512029.1:p.Met697=
XM_011513728.1:c.2078T= XP_011512030.1:p.Met693=
XM_011513729.1:c.2570T= XP_011512031.1:p.Met857=
XR_925155.1:n.2634T=
NM_001317924.1:c.2078T= NP_001304853.1:p.Met693=
XM_011513725.2:c.2504T= XP_011512027.1:p.Met835=
XM_011513726.3:c.2090T= XP_011512028.1:p.Met697=
XM_017008501.1:c.2078T= XP_016863990.1:p.Met693=
XR_001741306.1:n.2634T=
XR_001741307.1:n.2622T=
XR_001741308.1:n.2634T=
XR_001741309.1:n.2622T=
XR_001741310.1:n.2622T=
XR_001741311.2:n.2471T=
NM_025132.4:c.2558T= MANE Select NP_079408.3:p.Met853=
NM_001317924.2:c.2078T= NP_001304853.1:p.Met693=