Canonical Allele Identifier: CA1452063429

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244555A= , CM000666.2:g.39244555A=	GRCh38
NC_000004.11:g.39246175A= , CM000666.1:g.39246175A=	GRCh37
NC_000004.10:g.38922570A=	NCBI36
NG_031813.1:g.67152A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2645+3A= MANE Select	ENSP00000382717.3:n.2645+3A=
ENST00000399820.7:c.2645+3A=	ENSP00000382717.3:n.2645+3A=
ENST00000506869.5:c.*2226+3A=	ENSP00000424319.1:n.*2226+3A=
ENST00000512095.5:n.1643+3A=
NM_025132.3:c.2645+3A=	NP_079408.3:n.2645+3A=
XM_011513724.1:c.2657+3A=	XP_011512026.1:n.2657+3A=
XM_011513725.1:c.2591+3A=	XP_011512027.1:n.2591+3A=
XM_011513726.1:c.2177+3A=	XP_011512028.1:n.2177+3A=
XM_011513727.1:c.2177+3A=	XP_011512029.1:n.2177+3A=
XM_011513728.1:c.2165+3A=	XP_011512030.1:n.2165+3A=
XM_011513729.1:c.2657+3A=	XP_011512031.1:n.2657+3A=
XR_925155.1:n.2721+3A=
NM_001317924.1:c.2165+3A=	NP_001304853.1:n.2165+3A=
XM_011513725.2:c.2591+3A=	XP_011512027.1:n.2591+3A=
XM_011513726.3:c.2177+3A=	XP_011512028.1:n.2177+3A=
XM_017008501.1:c.2165+3A=	XP_016863990.1:n.2165+3A=
XR_001741306.1:n.2721+3A=
XR_001741307.1:n.2709+3A=
XR_001741308.1:n.2721+3A=
XR_001741309.1:n.2709+3A=
XR_001741310.1:n.2709+3A=
XR_001741311.2:n.2558+3A=
NM_025132.4:c.2645+3A= MANE Select	NP_079408.3:n.2645+3A=
NM_001317924.2:c.2165+3A=	NP_001304853.1:n.2165+3A=