Canonical Allele Identifier: CA1452056932

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39274957A= , CM000666.2:g.39274957A=	GRCh38
NC_000004.11:g.39276577A= , CM000666.1:g.39276577A=	GRCh37
NC_000004.10:g.38952972A=	NCBI36
NG_031813.1:g.97554A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3715A= MANE Select	ENSP00000382717.3:p.Arg1239=
ENST00000399820.7:c.3715A=	ENSP00000382717.3:p.Arg1239=
ENST00000506869.5:c.*3296A=	ENSP00000424319.1:n.*3296A=
ENST00000512095.5:n.2713A=
ENST00000512534.5:n.2026A=
NM_025132.3:c.3715A=	NP_079408.3:p.Arg1239=
XM_011513724.1:c.3727A=	XP_011512026.1:p.Arg1243=
XM_011513725.1:c.3661A=	XP_011512027.1:p.Arg1221=
XM_011513726.1:c.3247A=	XP_011512028.1:p.Arg1083=
XM_011513727.1:c.3247A=	XP_011512029.1:p.Arg1083=
XM_011513728.1:c.3235A=	XP_011512030.1:p.Arg1079=
XR_925155.1:n.5425A=
NM_001317924.1:c.3235A=	NP_001304853.1:p.Arg1079=
XM_011513725.2:c.3661A=	XP_011512027.1:p.Arg1221=
XM_011513726.3:c.3247A=	XP_011512028.1:p.Arg1083=
XM_017008501.1:c.3235A=	XP_016863990.1:p.Arg1079=
XR_001741306.1:n.3791A=
XR_001741307.1:n.3779A=
XR_001741308.1:n.5425A=
XR_001741309.1:n.5413A=
XR_001741310.1:n.5413A=
XR_001741311.2:n.5262A=
NM_025132.4:c.3715A= MANE Select	NP_079408.3:p.Arg1239=
NM_001317924.2:c.3235A=	NP_001304853.1:p.Arg1079=