Canonical Allele Identifier: CA1452063278

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244474T= , CM000666.2:g.39244474T=	GRCh38
NC_000004.11:g.39246094T= , CM000666.1:g.39246094T=	GRCh37
NC_000004.10:g.38922489T=	NCBI36
NG_031813.1:g.67071T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.2567T= MANE Select	ENSP00000382717.3:p.Phe856=
ENST00000399820.7:c.2567T=	ENSP00000382717.3:p.Phe856=
ENST00000506869.5:c.*2148T=	ENSP00000424319.1:n.*2148T=
ENST00000512095.5:n.1565T=
NM_025132.3:c.2567T=	NP_079408.3:p.Phe856=
XM_011513724.1:c.2579T=	XP_011512026.1:p.Phe860=
XM_011513725.1:c.2513T=	XP_011512027.1:p.Phe838=
XM_011513726.1:c.2099T=	XP_011512028.1:p.Phe700=
XM_011513727.1:c.2099T=	XP_011512029.1:p.Phe700=
XM_011513728.1:c.2087T=	XP_011512030.1:p.Phe696=
XM_011513729.1:c.2579T=	XP_011512031.1:p.Phe860=
XR_925155.1:n.2643T=
NM_001317924.1:c.2087T=	NP_001304853.1:p.Phe696=
XM_011513725.2:c.2513T=	XP_011512027.1:p.Phe838=
XM_011513726.3:c.2099T=	XP_011512028.1:p.Phe700=
XM_017008501.1:c.2087T=	XP_016863990.1:p.Phe696=
XR_001741306.1:n.2643T=
XR_001741307.1:n.2631T=
XR_001741308.1:n.2643T=
XR_001741309.1:n.2631T=
XR_001741310.1:n.2631T=
XR_001741311.2:n.2480T=
NM_025132.4:c.2567T= MANE Select	NP_079408.3:p.Phe856=
NM_001317924.2:c.2087T=	NP_001304853.1:p.Phe696=