Canonical Allele Identifier: CA356638243

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39246095T>G (hg19) ; chr4:g.39244475T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244475T>G , CM000666.2:g.39244475T>G	GRCh38
NC_000004.11:g.39246095T>G , CM000666.1:g.39246095T>G	GRCh37
NC_000004.10:g.38922490T>G	NCBI36
NG_031813.1:g.67072T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.2568T>G MANE Select	ENSP00000382717.3:p.Phe856Leu
ENST00000399820.7:c.2568T>G	ENSP00000382717.3:p.Phe856Leu
ENST00000506869.5:c.*2149T>G	ENSP00000424319.1:n.*2149T>G
ENST00000512095.5:n.1566T>G
NM_025132.3:c.2568T>G	NP_079408.3:p.Phe856Leu
XM_011513724.1:c.2580T>G	XP_011512026.1:p.Phe860Leu
XM_011513725.1:c.2514T>G	XP_011512027.1:p.Phe838Leu
XM_011513726.1:c.2100T>G	XP_011512028.1:p.Phe700Leu
XM_011513727.1:c.2100T>G	XP_011512029.1:p.Phe700Leu
XM_011513728.1:c.2088T>G	XP_011512030.1:p.Phe696Leu
XM_011513729.1:c.2580T>G	XP_011512031.1:p.Phe860Leu
XR_925155.1:n.2644T>G
NM_001317924.1:c.2088T>G	NP_001304853.1:p.Phe696Leu
XM_011513725.2:c.2514T>G	XP_011512027.1:p.Phe838Leu
XM_011513726.3:c.2100T>G	XP_011512028.1:p.Phe700Leu
XM_017008501.1:c.2088T>G	XP_016863990.1:p.Phe696Leu
XR_001741306.1:n.2644T>G
XR_001741307.1:n.2632T>G
XR_001741308.1:n.2644T>G
XR_001741309.1:n.2632T>G
XR_001741310.1:n.2632T>G
XR_001741311.2:n.2481T>G
NM_025132.4:c.2568T>G MANE Select	NP_079408.3:p.Phe856Leu
NM_001317924.2:c.2088T>G	NP_001304853.1:p.Phe696Leu