Canonical Allele Identifier: CA1452063321

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244485G= , CM000666.2:g.39244485G=	GRCh38
NC_000004.11:g.39246105G= , CM000666.1:g.39246105G=	GRCh37
NC_000004.10:g.38922500G=	NCBI36
NG_031813.1:g.67082G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2578G= MANE Select	ENSP00000382717.3:p.Ala860=
ENST00000399820.7:c.2578G=	ENSP00000382717.3:p.Ala860=
ENST00000506869.5:c.*2159G=	ENSP00000424319.1:n.*2159G=
ENST00000512095.5:n.1576G=
NM_025132.3:c.2578G=	NP_079408.3:p.Ala860=
XM_011513724.1:c.2590G=	XP_011512026.1:p.Ala864=
XM_011513725.1:c.2524G=	XP_011512027.1:p.Ala842=
XM_011513726.1:c.2110G=	XP_011512028.1:p.Ala704=
XM_011513727.1:c.2110G=	XP_011512029.1:p.Ala704=
XM_011513728.1:c.2098G=	XP_011512030.1:p.Ala700=
XM_011513729.1:c.2590G=	XP_011512031.1:p.Ala864=
XR_925155.1:n.2654G=
NM_001317924.1:c.2098G=	NP_001304853.1:p.Ala700=
XM_011513725.2:c.2524G=	XP_011512027.1:p.Ala842=
XM_011513726.3:c.2110G=	XP_011512028.1:p.Ala704=
XM_017008501.1:c.2098G=	XP_016863990.1:p.Ala700=
XR_001741306.1:n.2654G=
XR_001741307.1:n.2642G=
XR_001741308.1:n.2654G=
XR_001741309.1:n.2642G=
XR_001741310.1:n.2642G=
XR_001741311.2:n.2491G=
NM_025132.4:c.2578G= MANE Select	NP_079408.3:p.Ala860=
NM_001317924.2:c.2098G=	NP_001304853.1:p.Ala700=