Canonical Allele Identifier: CA1452057110

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275149G= , CM000666.2:g.39275149G=	GRCh38
NC_000004.11:g.39276769G= , CM000666.1:g.39276769G=	GRCh37
NC_000004.10:g.38953164G=	NCBI36
NG_031813.1:g.97746G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+191G= MANE Select	ENSP00000382717.3:n.3716+191G=
ENST00000399820.7:c.3716+191G=	ENSP00000382717.3:n.3716+191G=
ENST00000506869.5:c.*3297+191G=	ENSP00000424319.1:n.*3297+191G=
ENST00000512095.5:n.2905G=
ENST00000512534.5:n.2027+191G=
NM_025132.3:c.3716+191G=	NP_079408.3:n.3716+191G=
XM_011513724.1:c.3728+191G=	XP_011512026.1:n.3728+191G=
XM_011513725.1:c.3662+191G=	XP_011512027.1:n.3662+191G=
XM_011513726.1:c.3248+191G=	XP_011512028.1:n.3248+191G=
XM_011513727.1:c.3248+191G=	XP_011512029.1:n.3248+191G=
XM_011513728.1:c.3236+191G=	XP_011512030.1:n.3236+191G=
XR_925155.1:n.5426+191G=
NM_001317924.1:c.3236+191G=	NP_001304853.1:n.3236+191G=
XM_011513725.2:c.3662+191G=	XP_011512027.1:n.3662+191G=
XM_011513726.3:c.3248+191G=	XP_011512028.1:n.3248+191G=
XM_017008501.1:c.3236+191G=	XP_016863990.1:n.3236+191G=
XR_001741306.1:n.3792+191G=
XR_001741307.1:n.3780+191G=
XR_001741308.1:n.5426+191G=
XR_001741309.1:n.5414+191G=
XR_001741310.1:n.5414+191G=
XR_001741311.2:n.5263+191G=
NM_025132.4:c.3716+191G= MANE Select	NP_079408.3:n.3716+191G=
NM_001317924.2:c.3236+191G=	NP_001304853.1:n.3236+191G=