Canonical Allele Identifier: CA2892368

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39270033A>G , CM000666.2:g.39270033A>G	GRCh38
NC_000004.11:g.39271653A>G , CM000666.1:g.39271653A>G	GRCh37
NC_000004.10:g.38948048A>G	NCBI36
NG_031813.1:g.92630A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.3416A>G MANE Select	NP_079408.3:p.Gln1139Arg
ENST00000399820.8:c.3416A>G MANE Select	ENSP00000382717.3:p.Gln1139Arg
NM_001317924.1:c.2936A>G	NP_001304853.1:p.Gln979Arg
NM_001317924.2:c.2936A>G	NP_001304853.1:p.Gln979Arg
NM_025132.3:c.3416A>G	NP_079408.3:p.Gln1139Arg
ENST00000399820.7:c.3416A>G	ENSP00000382717.3:p.Gln1139Arg
ENST00000506869.5:c.*2997A>G	ENSP00000424319.1:n.*2997A>G
ENST00000512095.5:n.2414A>G
XM_011513724.1:c.3428A>G	XP_011512026.1:p.Gln1143Arg
XM_011513725.1:c.3362A>G	XP_011512027.1:p.Gln1121Arg
XM_011513725.2:c.3362A>G	XP_011512027.1:p.Gln1121Arg
XM_011513726.1:c.2948A>G	XP_011512028.1:p.Gln983Arg
XM_011513726.3:c.2948A>G	XP_011512028.1:p.Gln983Arg
XM_011513727.1:c.2948A>G	XP_011512029.1:p.Gln983Arg
XM_011513728.1:c.2936A>G	XP_011512030.1:p.Gln979Arg
XM_017008501.1:c.2936A>G	XP_016863990.1:p.Gln979Arg
XR_001741306.1:n.3492A>G
XR_001741307.1:n.3480A>G
XR_001741308.1:n.3492A>G
XR_001741309.1:n.3480A>G
XR_001741310.1:n.3480A>G
XR_001741311.2:n.3329A>G
XR_925155.1:n.3492A>G