Canonical Allele Identifier: CA2892447

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39274949G>A , CM000666.2:g.39274949G>A	GRCh38
NC_000004.11:g.39276569G>A , CM000666.1:g.39276569G>A	GRCh37
NC_000004.10:g.38952964G>A	NCBI36
NG_031813.1:g.97546G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3707G>A MANE Select	ENSP00000382717.3:p.Gly1236Glu
ENST00000399820.7:c.3707G>A	ENSP00000382717.3:p.Gly1236Glu
ENST00000506869.5:c.*3288G>A	ENSP00000424319.1:n.*3288G>A
ENST00000512095.5:n.2705G>A
ENST00000512534.5:n.2018G>A
NM_025132.3:c.3707G>A	NP_079408.3:p.Gly1236Glu
XM_011513724.1:c.3719G>A	XP_011512026.1:p.Gly1240Glu
XM_011513725.1:c.3653G>A	XP_011512027.1:p.Gly1218Glu
XM_011513726.1:c.3239G>A	XP_011512028.1:p.Gly1080Glu
XM_011513727.1:c.3239G>A	XP_011512029.1:p.Gly1080Glu
XM_011513728.1:c.3227G>A	XP_011512030.1:p.Gly1076Glu
XR_925155.1:n.5417G>A
NM_001317924.1:c.3227G>A	NP_001304853.1:p.Gly1076Glu
XM_011513725.2:c.3653G>A	XP_011512027.1:p.Gly1218Glu
XM_011513726.3:c.3239G>A	XP_011512028.1:p.Gly1080Glu
XM_017008501.1:c.3227G>A	XP_016863990.1:p.Gly1076Glu
XR_001741306.1:n.3783G>A
XR_001741307.1:n.3771G>A
XR_001741308.1:n.5417G>A
XR_001741309.1:n.5405G>A
XR_001741310.1:n.5405G>A
XR_001741311.2:n.5254G>A
NM_025132.4:c.3707G>A MANE Select	NP_079408.3:p.Gly1236Glu
NM_001317924.2:c.3227G>A	NP_001304853.1:p.Gly1076Glu