Canonical Allele Identifier: CA356637235
Gene: WDR19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39244248G>A , CM000666.2:g.39244248G>A GRCh38
NC_000004.11:g.39245868G>A , CM000666.1:g.39245868G>A GRCh37
NC_000004.10:g.38922263G>A NCBI36
NG_031813.1:g.66845G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399820.8:c.2422G>A MANE Select ENSP00000382717.3:p.Glu808Lys
ENST00000399820.7:c.2422G>A ENSP00000382717.3:p.Glu808Lys
ENST00000506869.5:c.*2003G>A ENSP00000424319.1:n.*2003G>A
ENST00000512095.5:n.1420G>A
NM_025132.3:c.2422G>A NP_079408.3:p.Glu808Lys
XM_011513724.1:c.2434G>A XP_011512026.1:p.Glu812Lys
XM_011513725.1:c.2368G>A XP_011512027.1:p.Glu790Lys
XM_011513726.1:c.1954G>A XP_011512028.1:p.Glu652Lys
XM_011513727.1:c.1954G>A XP_011512029.1:p.Glu652Lys
XM_011513728.1:c.1942G>A XP_011512030.1:p.Glu648Lys
XM_011513729.1:c.2434G>A XP_011512031.1:p.Glu812Lys
XR_925155.1:n.2498G>A
NM_001317924.1:c.1942G>A NP_001304853.1:p.Glu648Lys
XM_011513725.2:c.2368G>A XP_011512027.1:p.Glu790Lys
XM_011513726.3:c.1954G>A XP_011512028.1:p.Glu652Lys
XM_017008501.1:c.1942G>A XP_016863990.1:p.Glu648Lys
XR_001741306.1:n.2498G>A
XR_001741307.1:n.2486G>A
XR_001741308.1:n.2498G>A
XR_001741309.1:n.2486G>A
XR_001741310.1:n.2486G>A
XR_001741311.2:n.2335G>A
NM_025132.4:c.2422G>A MANE Select NP_079408.3:p.Glu808Lys
NM_001317924.2:c.1942G>A NP_001304853.1:p.Glu648Lys