Canonical Allele Identifier: CA1452055201

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273038A= , CM000666.2:g.39273038A=	GRCh38
NC_000004.11:g.39274658A= , CM000666.1:g.39274658A=	GRCh37
NC_000004.10:g.38951053A=	NCBI36
NG_031813.1:g.95635A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3542A= MANE Select	ENSP00000382717.3:p.Asn1181=
ENST00000399820.7:c.3542A=	ENSP00000382717.3:p.Asn1181=
ENST00000506869.5:c.*3123A=	ENSP00000424319.1:n.*3123A=
ENST00000512095.5:n.2540A=
ENST00000512534.5:n.107A=
NM_025132.3:c.3542A=	NP_079408.3:p.Asn1181=
XM_011513724.1:c.3554A=	XP_011512026.1:p.Asn1185=
XM_011513725.1:c.3488A=	XP_011512027.1:p.Asn1163=
XM_011513726.1:c.3074A=	XP_011512028.1:p.Asn1025=
XM_011513727.1:c.3074A=	XP_011512029.1:p.Asn1025=
XM_011513728.1:c.3062A=	XP_011512030.1:p.Asn1021=
XR_925155.1:n.3618A=
NM_001317924.1:c.3062A=	NP_001304853.1:p.Asn1021=
XM_011513725.2:c.3488A=	XP_011512027.1:p.Asn1163=
XM_011513726.3:c.3074A=	XP_011512028.1:p.Asn1025=
XM_017008501.1:c.3062A=	XP_016863990.1:p.Asn1021=
XR_001741306.1:n.3618A=
XR_001741307.1:n.3606A=
XR_001741308.1:n.3618A=
XR_001741309.1:n.3606A=
XR_001741310.1:n.3606A=
XR_001741311.2:n.3455A=
NM_025132.4:c.3542A= MANE Select	NP_079408.3:p.Asn1181=
NM_001317924.2:c.3062A=	NP_001304853.1:p.Asn1021=