Canonical Allele Identifier: CA1452062989

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244318T= , CM000666.2:g.39244318T=	GRCh38
NC_000004.11:g.39245938T= , CM000666.1:g.39245938T=	GRCh37
NC_000004.10:g.38922333T=	NCBI36
NG_031813.1:g.66915T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2492T= MANE Select	ENSP00000382717.3:p.Val831=
ENST00000399820.7:c.2492T=	ENSP00000382717.3:p.Val831=
ENST00000506869.5:c.*2073T=	ENSP00000424319.1:n.*2073T=
ENST00000512095.5:n.1490T=
NM_025132.3:c.2492T=	NP_079408.3:p.Val831=
XM_011513724.1:c.2504T=	XP_011512026.1:p.Val835=
XM_011513725.1:c.2438T=	XP_011512027.1:p.Val813=
XM_011513726.1:c.2024T=	XP_011512028.1:p.Val675=
XM_011513727.1:c.2024T=	XP_011512029.1:p.Val675=
XM_011513728.1:c.2012T=	XP_011512030.1:p.Val671=
XM_011513729.1:c.2504T=	XP_011512031.1:p.Val835=
XR_925155.1:n.2568T=
NM_001317924.1:c.2012T=	NP_001304853.1:p.Val671=
XM_011513725.2:c.2438T=	XP_011512027.1:p.Val813=
XM_011513726.3:c.2024T=	XP_011512028.1:p.Val675=
XM_017008501.1:c.2012T=	XP_016863990.1:p.Val671=
XR_001741306.1:n.2568T=
XR_001741307.1:n.2556T=
XR_001741308.1:n.2568T=
XR_001741309.1:n.2556T=
XR_001741310.1:n.2556T=
XR_001741311.2:n.2405T=
NM_025132.4:c.2492T= MANE Select	NP_079408.3:p.Val831=
NM_001317924.2:c.2012T=	NP_001304853.1:p.Val671=