Canonical Allele Identifier: CA1452063085

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244392C= , CM000666.2:g.39244392C=	GRCh38
NC_000004.11:g.39246012C= , CM000666.1:g.39246012C=	GRCh37
NC_000004.10:g.38922407C=	NCBI36
NG_031813.1:g.66989C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.2562+4C= MANE Select	ENSP00000382717.3:n.2562+4C=
ENST00000399820.7:c.2562+4C=	ENSP00000382717.3:n.2562+4C=
ENST00000506869.5:c.*2143+4C=	ENSP00000424319.1:n.*2143+4C=
ENST00000512095.5:n.1560+4C=
NM_025132.3:c.2562+4C=	NP_079408.3:n.2562+4C=
XM_011513724.1:c.2574+4C=	XP_011512026.1:n.2574+4C=
XM_011513725.1:c.2508+4C=	XP_011512027.1:n.2508+4C=
XM_011513726.1:c.2094+4C=	XP_011512028.1:n.2094+4C=
XM_011513727.1:c.2094+4C=	XP_011512029.1:n.2094+4C=
XM_011513728.1:c.2082+4C=	XP_011512030.1:n.2082+4C=
XM_011513729.1:c.2574+4C=	XP_011512031.1:n.2574+4C=
XR_925155.1:n.2638+4C=
NM_001317924.1:c.2082+4C=	NP_001304853.1:n.2082+4C=
XM_011513725.2:c.2508+4C=	XP_011512027.1:n.2508+4C=
XM_011513726.3:c.2094+4C=	XP_011512028.1:n.2094+4C=
XM_017008501.1:c.2082+4C=	XP_016863990.1:n.2082+4C=
XR_001741306.1:n.2638+4C=
XR_001741307.1:n.2626+4C=
XR_001741308.1:n.2638+4C=
XR_001741309.1:n.2626+4C=
XR_001741310.1:n.2626+4C=
XR_001741311.2:n.2475+4C=
NM_025132.4:c.2562+4C= MANE Select	NP_079408.3:n.2562+4C=
NM_001317924.2:c.2082+4C=	NP_001304853.1:n.2082+4C=