Canonical Allele Identifier: CA1451994631

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205592T= , CM000666.2:g.39205592T=	GRCh38
NC_000004.11:g.39207212T= , CM000666.1:g.39207212T=	GRCh37
NC_000004.10:g.38883607T=	NCBI36
NG_031813.1:g.28189T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.746T= MANE Select	ENSP00000382717.3:p.Phe249=
ENST00000399820.7:c.746T=	ENSP00000382717.3:p.Phe249=
ENST00000503697.5:c.*214T=	ENSP00000423706.1:n.*214T=
ENST00000506503.1:c.746T=	ENSP00000423491.1:p.Phe249=
ENST00000506869.5:c.*327T=	ENSP00000424319.1:n.*327T=
ENST00000511729.5:n.41-22966T=
ENST00000512448.1:n.340T=
NM_025132.3:c.746T=	NP_079408.3:p.Phe249=
XM_011513724.1:c.746T=	XP_011512026.1:p.Phe249=
XM_011513725.1:c.680T=	XP_011512027.1:p.Phe227=
XM_011513726.1:c.266T=	XP_011512028.1:p.Phe89=
XM_011513727.1:c.266T=	XP_011512029.1:p.Phe89=
XM_011513728.1:c.266T=	XP_011512030.1:p.Phe89=
XM_011513729.1:c.746T=	XP_011512031.1:p.Phe249=
XR_925155.1:n.810T=
NM_001317924.1:c.266T=	NP_001304853.1:p.Phe89=
XM_011513725.2:c.680T=	XP_011512027.1:p.Phe227=
XM_011513726.3:c.266T=	XP_011512028.1:p.Phe89=
XM_017008501.1:c.266T=	XP_016863990.1:p.Phe89=
XR_001741306.1:n.810T=
XR_001741307.1:n.810T=
XR_001741308.1:n.810T=
XR_001741309.1:n.810T=
XR_001741310.1:n.810T=
XR_001741311.2:n.659T=
XR_001741312.1:n.810T=
NM_025132.4:c.746T= MANE Select	NP_079408.3:p.Phe249=
NM_001317924.2:c.266T=	NP_001304853.1:p.Phe89=