Canonical Allele Identifier: CA1451994674

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205617T= , CM000666.2:g.39205617T=	GRCh38
NC_000004.11:g.39207237T= , CM000666.1:g.39207237T=	GRCh37
NC_000004.10:g.38883632T=	NCBI36
NG_031813.1:g.28214T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.771T= MANE Select	ENSP00000382717.3:p.Ile257=
ENST00000399820.7:c.771T=	ENSP00000382717.3:p.Ile257=
ENST00000503697.5:c.*239T=	ENSP00000423706.1:n.*239T=
ENST00000506503.1:c.771T=	ENSP00000423491.1:p.Ile257=
ENST00000506869.5:c.*352T=	ENSP00000424319.1:n.*352T=
ENST00000511729.5:n.41-22941T=
ENST00000512448.1:n.365T=
NM_025132.3:c.771T=	NP_079408.3:p.Ile257=
XM_011513724.1:c.771T=	XP_011512026.1:p.Ile257=
XM_011513725.1:c.705T=	XP_011512027.1:p.Ile235=
XM_011513726.1:c.291T=	XP_011512028.1:p.Ile97=
XM_011513727.1:c.291T=	XP_011512029.1:p.Ile97=
XM_011513728.1:c.291T=	XP_011512030.1:p.Ile97=
XM_011513729.1:c.771T=	XP_011512031.1:p.Ile257=
XR_925155.1:n.835T=
NM_001317924.1:c.291T=	NP_001304853.1:p.Ile97=
XM_011513725.2:c.705T=	XP_011512027.1:p.Ile235=
XM_011513726.3:c.291T=	XP_011512028.1:p.Ile97=
XM_017008501.1:c.291T=	XP_016863990.1:p.Ile97=
XR_001741306.1:n.835T=
XR_001741307.1:n.835T=
XR_001741308.1:n.835T=
XR_001741309.1:n.835T=
XR_001741310.1:n.835T=
XR_001741311.2:n.684T=
XR_001741312.1:n.835T=
NM_025132.4:c.771T= MANE Select	NP_079408.3:p.Ile257=
NM_001317924.2:c.291T=	NP_001304853.1:p.Ile97=