Canonical Allele Identifier: CA356638229

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39246093T>A (hg19) ; chr4:g.39244473T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244473T>A , CM000666.2:g.39244473T>A	GRCh38
NC_000004.11:g.39246093T>A , CM000666.1:g.39246093T>A	GRCh37
NC_000004.10:g.38922488T>A	NCBI36
NG_031813.1:g.67070T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.2566T>A MANE Select	ENSP00000382717.3:p.Phe856Ile
ENST00000399820.7:c.2566T>A	ENSP00000382717.3:p.Phe856Ile
ENST00000506869.5:c.*2147T>A	ENSP00000424319.1:n.*2147T>A
ENST00000512095.5:n.1564T>A
NM_025132.3:c.2566T>A	NP_079408.3:p.Phe856Ile
XM_011513724.1:c.2578T>A	XP_011512026.1:p.Phe860Ile
XM_011513725.1:c.2512T>A	XP_011512027.1:p.Phe838Ile
XM_011513726.1:c.2098T>A	XP_011512028.1:p.Phe700Ile
XM_011513727.1:c.2098T>A	XP_011512029.1:p.Phe700Ile
XM_011513728.1:c.2086T>A	XP_011512030.1:p.Phe696Ile
XM_011513729.1:c.2578T>A	XP_011512031.1:p.Phe860Ile
XR_925155.1:n.2642T>A
NM_001317924.1:c.2086T>A	NP_001304853.1:p.Phe696Ile
XM_011513725.2:c.2512T>A	XP_011512027.1:p.Phe838Ile
XM_011513726.3:c.2098T>A	XP_011512028.1:p.Phe700Ile
XM_017008501.1:c.2086T>A	XP_016863990.1:p.Phe696Ile
XR_001741306.1:n.2642T>A
XR_001741307.1:n.2630T>A
XR_001741308.1:n.2642T>A
XR_001741309.1:n.2630T>A
XR_001741310.1:n.2630T>A
XR_001741311.2:n.2479T>A
NM_025132.4:c.2566T>A MANE Select	NP_079408.3:p.Phe856Ile
NM_001317924.2:c.2086T>A	NP_001304853.1:p.Phe696Ile