Canonical Allele Identifier: CA1452063336

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244492T= , CM000666.2:g.39244492T=	GRCh38
NC_000004.11:g.39246112T= , CM000666.1:g.39246112T=	GRCh37
NC_000004.10:g.38922507T=	NCBI36
NG_031813.1:g.67089T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2585T= MANE Select	ENSP00000382717.3:p.Leu862=
ENST00000399820.7:c.2585T=	ENSP00000382717.3:p.Leu862=
ENST00000506869.5:c.*2166T=	ENSP00000424319.1:n.*2166T=
ENST00000512095.5:n.1583T=
NM_025132.3:c.2585T=	NP_079408.3:p.Leu862=
XM_011513724.1:c.2597T=	XP_011512026.1:p.Leu866=
XM_011513725.1:c.2531T=	XP_011512027.1:p.Leu844=
XM_011513726.1:c.2117T=	XP_011512028.1:p.Leu706=
XM_011513727.1:c.2117T=	XP_011512029.1:p.Leu706=
XM_011513728.1:c.2105T=	XP_011512030.1:p.Leu702=
XM_011513729.1:c.2597T=	XP_011512031.1:p.Leu866=
XR_925155.1:n.2661T=
NM_001317924.1:c.2105T=	NP_001304853.1:p.Leu702=
XM_011513725.2:c.2531T=	XP_011512027.1:p.Leu844=
XM_011513726.3:c.2117T=	XP_011512028.1:p.Leu706=
XM_017008501.1:c.2105T=	XP_016863990.1:p.Leu702=
XR_001741306.1:n.2661T=
XR_001741307.1:n.2649T=
XR_001741308.1:n.2661T=
XR_001741309.1:n.2649T=
XR_001741310.1:n.2649T=
XR_001741311.2:n.2498T=
NM_025132.4:c.2585T= MANE Select	NP_079408.3:p.Leu862=
NM_001317924.2:c.2105T=	NP_001304853.1:p.Leu702=