Canonical Allele Identifier: CA1452055157

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273016C= , CM000666.2:g.39273016C=	GRCh38
NC_000004.11:g.39274636C= , CM000666.1:g.39274636C=	GRCh37
NC_000004.10:g.38951031C=	NCBI36
NG_031813.1:g.95613C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3520C= MANE Select	ENSP00000382717.3:p.Arg1174=
ENST00000399820.7:c.3520C=	ENSP00000382717.3:p.Arg1174=
ENST00000506869.5:c.*3101C=	ENSP00000424319.1:n.*3101C=
ENST00000512095.5:n.2518C=
ENST00000512534.5:n.85C=
NM_025132.3:c.3520C=	NP_079408.3:p.Arg1174=
XM_011513724.1:c.3532C=	XP_011512026.1:p.Arg1178=
XM_011513725.1:c.3466C=	XP_011512027.1:p.Arg1156=
XM_011513726.1:c.3052C=	XP_011512028.1:p.Arg1018=
XM_011513727.1:c.3052C=	XP_011512029.1:p.Arg1018=
XM_011513728.1:c.3040C=	XP_011512030.1:p.Arg1014=
XR_925155.1:n.3596C=
NM_001317924.1:c.3040C=	NP_001304853.1:p.Arg1014=
XM_011513725.2:c.3466C=	XP_011512027.1:p.Arg1156=
XM_011513726.3:c.3052C=	XP_011512028.1:p.Arg1018=
XM_017008501.1:c.3040C=	XP_016863990.1:p.Arg1014=
XR_001741306.1:n.3596C=
XR_001741307.1:n.3584C=
XR_001741308.1:n.3596C=
XR_001741309.1:n.3584C=
XR_001741310.1:n.3584C=
XR_001741311.2:n.3433C=
NM_025132.4:c.3520C= MANE Select	NP_079408.3:p.Arg1174=
NM_001317924.2:c.3040C=	NP_001304853.1:p.Arg1014=