Canonical Allele Identifier: CA1451994288

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205241T= , CM000666.2:g.39205241T=	GRCh38
NC_000004.11:g.39206861T= , CM000666.1:g.39206861T=	GRCh37
NC_000004.10:g.38883256T=	NCBI36
NG_031813.1:g.27838T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.691T= MANE Select	ENSP00000382717.3:p.Phe231=
ENST00000399820.7:c.691T=	ENSP00000382717.3:p.Phe231=
ENST00000503697.5:c.*159T=	ENSP00000423706.1:n.*159T=
ENST00000505055.5:c.*272T=	ENSP00000425949.1:n.*272T=
ENST00000506503.1:c.691T=	ENSP00000423491.1:p.Phe231=
ENST00000506869.5:c.*272T=	ENSP00000424319.1:n.*272T=
ENST00000511729.5:n.40+22678T=
ENST00000512448.1:n.285T=
NM_025132.3:c.691T=	NP_079408.3:p.Phe231=
XM_011513724.1:c.691T=	XP_011512026.1:p.Phe231=
XM_011513725.1:c.625T=	XP_011512027.1:p.Phe209=
XM_011513726.1:c.211T=	XP_011512028.1:p.Phe71=
XM_011513727.1:c.211T=	XP_011512029.1:p.Phe71=
XM_011513728.1:c.211T=	XP_011512030.1:p.Phe71=
XM_011513729.1:c.691T=	XP_011512031.1:p.Phe231=
XR_925155.1:n.755T=
NM_001317924.1:c.211T=	NP_001304853.1:p.Phe71=
XM_011513725.2:c.625T=	XP_011512027.1:p.Phe209=
XM_011513726.3:c.211T=	XP_011512028.1:p.Phe71=
XM_017008501.1:c.211T=	XP_016863990.1:p.Phe71=
XR_001741306.1:n.755T=
XR_001741307.1:n.755T=
XR_001741308.1:n.755T=
XR_001741309.1:n.755T=
XR_001741310.1:n.755T=
XR_001741311.2:n.604T=
XR_001741312.1:n.755T=
NM_025132.4:c.691T= MANE Select	NP_079408.3:p.Phe231=
NM_001317924.2:c.211T=	NP_001304853.1:p.Phe71=