Canonical Allele Identifier: CA1452063057

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244374T= , CM000666.2:g.39244374T=	GRCh38
NC_000004.11:g.39245994T= , CM000666.1:g.39245994T=	GRCh37
NC_000004.10:g.38922389T=	NCBI36
NG_031813.1:g.66971T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.2548T= MANE Select	ENSP00000382717.3:p.Leu850=
ENST00000399820.7:c.2548T=	ENSP00000382717.3:p.Leu850=
ENST00000506869.5:c.*2129T=	ENSP00000424319.1:n.*2129T=
ENST00000512095.5:n.1546T=
NM_025132.3:c.2548T=	NP_079408.3:p.Leu850=
XM_011513724.1:c.2560T=	XP_011512026.1:p.Leu854=
XM_011513725.1:c.2494T=	XP_011512027.1:p.Leu832=
XM_011513726.1:c.2080T=	XP_011512028.1:p.Leu694=
XM_011513727.1:c.2080T=	XP_011512029.1:p.Leu694=
XM_011513728.1:c.2068T=	XP_011512030.1:p.Leu690=
XM_011513729.1:c.2560T=	XP_011512031.1:p.Leu854=
XR_925155.1:n.2624T=
NM_001317924.1:c.2068T=	NP_001304853.1:p.Leu690=
XM_011513725.2:c.2494T=	XP_011512027.1:p.Leu832=
XM_011513726.3:c.2080T=	XP_011512028.1:p.Leu694=
XM_017008501.1:c.2068T=	XP_016863990.1:p.Leu690=
XR_001741306.1:n.2624T=
XR_001741307.1:n.2612T=
XR_001741308.1:n.2624T=
XR_001741309.1:n.2612T=
XR_001741310.1:n.2612T=
XR_001741311.2:n.2461T=
NM_025132.4:c.2548T= MANE Select	NP_079408.3:p.Leu850=
NM_001317924.2:c.2068T=	NP_001304853.1:p.Leu690=