Canonical Allele Identifier: CA2838490455

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39276935C>A , CM000666.2:g.39276935C>A	GRCh38
NC_000004.11:g.39278555C>A , CM000666.1:g.39278555C>A	GRCh37
NC_000004.10:g.38954950C>A	NCBI36
NG_031813.1:g.99532C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3717-85C>A MANE Select	ENSP00000382717.3:n.3717-85C>A
ENST00000399820.7:c.3717-85C>A	ENSP00000382717.3:n.3717-85C>A
ENST00000506869.5:c.*3298-85C>A	ENSP00000424319.1:n.*3298-85C>A
ENST00000512534.5:n.2028-85C>A
NM_025132.3:c.3717-85C>A	NP_079408.3:n.3717-85C>A
XM_011513724.1:c.3729-85C>A	XP_011512026.1:n.3729-85C>A
XM_011513725.1:c.3663-85C>A	XP_011512027.1:n.3663-85C>A
XM_011513726.1:c.3249-85C>A	XP_011512028.1:n.3249-85C>A
XM_011513727.1:c.3249-85C>A	XP_011512029.1:n.3249-85C>A
XM_011513728.1:c.3237-85C>A	XP_011512030.1:n.3237-85C>A
XR_925155.1:n.5427-85C>A
NM_001317924.1:c.3237-85C>A	NP_001304853.1:n.3237-85C>A
XM_011513725.2:c.3663-85C>A	XP_011512027.1:n.3663-85C>A
XM_011513726.3:c.3249-85C>A	XP_011512028.1:n.3249-85C>A
XM_017008501.1:c.3237-85C>A	XP_016863990.1:n.3237-85C>A
XR_001741306.1:n.3993+56C>A
XR_001741307.1:n.3981+56C>A
XR_001741308.1:n.5627+56C>A
XR_001741309.1:n.5415-85C>A
XR_001741310.1:n.5615+56C>A
XR_001741311.2:n.5264-85C>A
NM_025132.4:c.3717-85C>A MANE Select	NP_079408.3:n.3717-85C>A
NM_001317924.2:c.3237-85C>A	NP_001304853.1:n.3237-85C>A