Canonical Allele Identifier: CA356647072

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39274603C>A (hg19) ; chr4:g.39272983C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39272983C>A , CM000666.2:g.39272983C>A	GRCh38
NC_000004.11:g.39274603C>A , CM000666.1:g.39274603C>A	GRCh37
NC_000004.10:g.38950998C>A	NCBI36
NG_031813.1:g.95580C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3487C>A MANE Select	ENSP00000382717.3:p.His1163Asn
ENST00000399820.7:c.3487C>A	ENSP00000382717.3:p.His1163Asn
ENST00000506869.5:c.*3068C>A	ENSP00000424319.1:n.*3068C>A
ENST00000512095.5:n.2485C>A
ENST00000512534.5:n.52C>A
NM_025132.3:c.3487C>A	NP_079408.3:p.His1163Asn
XM_011513724.1:c.3499C>A	XP_011512026.1:p.His1167Asn
XM_011513725.1:c.3433C>A	XP_011512027.1:p.His1145Asn
XM_011513726.1:c.3019C>A	XP_011512028.1:p.His1007Asn
XM_011513727.1:c.3019C>A	XP_011512029.1:p.His1007Asn
XM_011513728.1:c.3007C>A	XP_011512030.1:p.His1003Asn
XR_925155.1:n.3563C>A
NM_001317924.1:c.3007C>A	NP_001304853.1:p.His1003Asn
XM_011513725.2:c.3433C>A	XP_011512027.1:p.His1145Asn
XM_011513726.3:c.3019C>A	XP_011512028.1:p.His1007Asn
XM_017008501.1:c.3007C>A	XP_016863990.1:p.His1003Asn
XR_001741306.1:n.3563C>A
XR_001741307.1:n.3551C>A
XR_001741308.1:n.3563C>A
XR_001741309.1:n.3551C>A
XR_001741310.1:n.3551C>A
XR_001741311.2:n.3400C>A
NM_025132.4:c.3487C>A MANE Select	NP_079408.3:p.His1163Asn
NM_001317924.2:c.3007C>A	NP_001304853.1:p.His1003Asn