Canonical Allele Identifier: CA1452063021

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244354A= , CM000666.2:g.39244354A=	GRCh38
NC_000004.11:g.39245974A= , CM000666.1:g.39245974A=	GRCh37
NC_000004.10:g.38922369A=	NCBI36
NG_031813.1:g.66951A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2528A= MANE Select	ENSP00000382717.3:p.Lys843=
ENST00000399820.7:c.2528A=	ENSP00000382717.3:p.Lys843=
ENST00000506869.5:c.*2109A=	ENSP00000424319.1:n.*2109A=
ENST00000512095.5:n.1526A=
NM_025132.3:c.2528A=	NP_079408.3:p.Lys843=
XM_011513724.1:c.2540A=	XP_011512026.1:p.Lys847=
XM_011513725.1:c.2474A=	XP_011512027.1:p.Lys825=
XM_011513726.1:c.2060A=	XP_011512028.1:p.Lys687=
XM_011513727.1:c.2060A=	XP_011512029.1:p.Lys687=
XM_011513728.1:c.2048A=	XP_011512030.1:p.Lys683=
XM_011513729.1:c.2540A=	XP_011512031.1:p.Lys847=
XR_925155.1:n.2604A=
NM_001317924.1:c.2048A=	NP_001304853.1:p.Lys683=
XM_011513725.2:c.2474A=	XP_011512027.1:p.Lys825=
XM_011513726.3:c.2060A=	XP_011512028.1:p.Lys687=
XM_017008501.1:c.2048A=	XP_016863990.1:p.Lys683=
XR_001741306.1:n.2604A=
XR_001741307.1:n.2592A=
XR_001741308.1:n.2604A=
XR_001741309.1:n.2592A=
XR_001741310.1:n.2592A=
XR_001741311.2:n.2441A=
NM_025132.4:c.2528A= MANE Select	NP_079408.3:p.Lys843=
NM_001317924.2:c.2048A=	NP_001304853.1:p.Lys683=