Canonical Allele Identifier: CA356651027
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 446639
ClinVar RCV Id: RCV000515837
dbSNP Id: rs1191056931

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39274959G>A , CM000666.2:g.39274959G>A GRCh38
NC_000004.11:g.39276579G>A , CM000666.1:g.39276579G>A GRCh37
NC_000004.10:g.38952974G>A NCBI36
NG_031813.1:g.97556G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3716+1G>A MANE Select ENSP00000382717.3:n.3716+1G>A
ENST00000399820.7:c.3716+1G>A ENSP00000382717.3:n.3716+1G>A
ENST00000506869.5:c.*3297+1G>A ENSP00000424319.1:n.*3297+1G>A
ENST00000512095.5:n.2715G>A
ENST00000512534.5:n.2027+1G>A
NM_025132.3:c.3716+1G>A NP_079408.3:n.3716+1G>A
XM_011513724.1:c.3728+1G>A XP_011512026.1:n.3728+1G>A
XM_011513725.1:c.3662+1G>A XP_011512027.1:n.3662+1G>A
XM_011513726.1:c.3248+1G>A XP_011512028.1:n.3248+1G>A
XM_011513727.1:c.3248+1G>A XP_011512029.1:n.3248+1G>A
XM_011513728.1:c.3236+1G>A XP_011512030.1:n.3236+1G>A
XR_925155.1:n.5426+1G>A
NM_001317924.1:c.3236+1G>A NP_001304853.1:n.3236+1G>A
XM_011513725.2:c.3662+1G>A XP_011512027.1:n.3662+1G>A
XM_011513726.3:c.3248+1G>A XP_011512028.1:n.3248+1G>A
XM_017008501.1:c.3236+1G>A XP_016863990.1:n.3236+1G>A
XR_001741306.1:n.3792+1G>A
XR_001741307.1:n.3780+1G>A
XR_001741308.1:n.5426+1G>A
XR_001741309.1:n.5414+1G>A
XR_001741310.1:n.5414+1G>A
XR_001741311.2:n.5263+1G>A
NM_025132.4:c.3716+1G>A MANE Select NP_079408.3:n.3716+1G>A
NM_001317924.2:c.3236+1G>A NP_001304853.1:n.3236+1G>A