Canonical Allele Identifier: CA1452057129

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275180A= , CM000666.2:g.39275180A=	GRCh38
NC_000004.11:g.39276800A= , CM000666.1:g.39276800A=	GRCh37
NC_000004.10:g.38953195A=	NCBI36
NG_031813.1:g.97777A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+222A= MANE Select	ENSP00000382717.3:n.3716+222A=
ENST00000399820.7:c.3716+222A=	ENSP00000382717.3:n.3716+222A=
ENST00000506869.5:c.*3297+222A=	ENSP00000424319.1:n.*3297+222A=
ENST00000512095.5:n.2936A=
ENST00000512534.5:n.2027+222A=
NM_025132.3:c.3716+222A=	NP_079408.3:n.3716+222A=
XM_011513724.1:c.3728+222A=	XP_011512026.1:n.3728+222A=
XM_011513725.1:c.3662+222A=	XP_011512027.1:n.3662+222A=
XM_011513726.1:c.3248+222A=	XP_011512028.1:n.3248+222A=
XM_011513727.1:c.3248+222A=	XP_011512029.1:n.3248+222A=
XM_011513728.1:c.3236+222A=	XP_011512030.1:n.3236+222A=
XR_925155.1:n.5426+222A=
NM_001317924.1:c.3236+222A=	NP_001304853.1:n.3236+222A=
XM_011513725.2:c.3662+222A=	XP_011512027.1:n.3662+222A=
XM_011513726.3:c.3248+222A=	XP_011512028.1:n.3248+222A=
XM_017008501.1:c.3236+222A=	XP_016863990.1:n.3236+222A=
XR_001741306.1:n.3792+222A=
XR_001741307.1:n.3780+222A=
XR_001741308.1:n.5426+222A=
XR_001741309.1:n.5414+222A=
XR_001741310.1:n.5414+222A=
XR_001741311.2:n.5263+222A=
NM_025132.4:c.3716+222A= MANE Select	NP_079408.3:n.3716+222A=
NM_001317924.2:c.3236+222A=	NP_001304853.1:n.3236+222A=