Canonical Allele Identifier: CA1451994692

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205626T= , CM000666.2:g.39205626T=	GRCh38
NC_000004.11:g.39207246T= , CM000666.1:g.39207246T=	GRCh37
NC_000004.10:g.38883641T=	NCBI36
NG_031813.1:g.28223T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.780T= MANE Select	ENSP00000382717.3:p.His260=
ENST00000399820.7:c.780T=	ENSP00000382717.3:p.His260=
ENST00000503697.5:c.*248T=	ENSP00000423706.1:n.*248T=
ENST00000506503.1:c.780T=	ENSP00000423491.1:p.His260=
ENST00000506869.5:c.*361T=	ENSP00000424319.1:n.*361T=
ENST00000511729.5:n.41-22932T=
ENST00000512448.1:n.374T=
NM_025132.3:c.780T=	NP_079408.3:p.His260=
XM_011513724.1:c.780T=	XP_011512026.1:p.His260=
XM_011513725.1:c.714T=	XP_011512027.1:p.His238=
XM_011513726.1:c.300T=	XP_011512028.1:p.His100=
XM_011513727.1:c.300T=	XP_011512029.1:p.His100=
XM_011513728.1:c.300T=	XP_011512030.1:p.His100=
XM_011513729.1:c.780T=	XP_011512031.1:p.His260=
XR_925155.1:n.844T=
NM_001317924.1:c.300T=	NP_001304853.1:p.His100=
XM_011513725.2:c.714T=	XP_011512027.1:p.His238=
XM_011513726.3:c.300T=	XP_011512028.1:p.His100=
XM_017008501.1:c.300T=	XP_016863990.1:p.His100=
XR_001741306.1:n.844T=
XR_001741307.1:n.844T=
XR_001741308.1:n.844T=
XR_001741309.1:n.844T=
XR_001741310.1:n.844T=
XR_001741311.2:n.693T=
XR_001741312.1:n.844T=
NM_025132.4:c.780T= MANE Select	NP_079408.3:p.His260=
NM_001317924.2:c.300T=	NP_001304853.1:p.His100=