Canonical Allele Identifier: CA1451994648

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205596A= , CM000666.2:g.39205596A=	GRCh38
NC_000004.11:g.39207216A= , CM000666.1:g.39207216A=	GRCh37
NC_000004.10:g.38883611A=	NCBI36
NG_031813.1:g.28193A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.750A= MANE Select	ENSP00000382717.3:p.Ser250=
ENST00000399820.7:c.750A=	ENSP00000382717.3:p.Ser250=
ENST00000503697.5:c.*218A=	ENSP00000423706.1:n.*218A=
ENST00000506503.1:c.750A=	ENSP00000423491.1:p.Ser250=
ENST00000506869.5:c.*331A=	ENSP00000424319.1:n.*331A=
ENST00000511729.5:n.41-22962A=
ENST00000512448.1:n.344A=
NM_025132.3:c.750A=	NP_079408.3:p.Ser250=
XM_011513724.1:c.750A=	XP_011512026.1:p.Ser250=
XM_011513725.1:c.684A=	XP_011512027.1:p.Ser228=
XM_011513726.1:c.270A=	XP_011512028.1:p.Ser90=
XM_011513727.1:c.270A=	XP_011512029.1:p.Ser90=
XM_011513728.1:c.270A=	XP_011512030.1:p.Ser90=
XM_011513729.1:c.750A=	XP_011512031.1:p.Ser250=
XR_925155.1:n.814A=
NM_001317924.1:c.270A=	NP_001304853.1:p.Ser90=
XM_011513725.2:c.684A=	XP_011512027.1:p.Ser228=
XM_011513726.3:c.270A=	XP_011512028.1:p.Ser90=
XM_017008501.1:c.270A=	XP_016863990.1:p.Ser90=
XR_001741306.1:n.814A=
XR_001741307.1:n.814A=
XR_001741308.1:n.814A=
XR_001741309.1:n.814A=
XR_001741310.1:n.814A=
XR_001741311.2:n.663A=
XR_001741312.1:n.814A=
NM_025132.4:c.750A= MANE Select	NP_079408.3:p.Ser250=
NM_001317924.2:c.270A=	NP_001304853.1:p.Ser90=