Canonical Allele Identifier: CA2891921

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39228355A>G , CM000666.2:g.39228355A>G	GRCh38
NC_000004.11:g.39229975A>G , CM000666.1:g.39229975A>G	GRCh37
NC_000004.10:g.38906370A>G	NCBI36
NG_031813.1:g.50952A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.1775A>G MANE Select	NP_079408.3:p.Gln592Arg
ENST00000399820.8:c.1775A>G MANE Select	ENSP00000382717.3:p.Gln592Arg
NM_001317924.1:c.1295A>G	NP_001304853.1:p.Gln432Arg
NM_001317924.2:c.1295A>G	NP_001304853.1:p.Gln432Arg
NM_025132.3:c.1775A>G	NP_079408.3:p.Gln592Arg
ENST00000399820.7:c.1775A>G	ENSP00000382717.3:p.Gln592Arg
ENST00000506869.5:c.*1356A>G	ENSP00000424319.1:n.*1356A>G
ENST00000511729.5:n.41-203A>G
ENST00000512095.5:n.773A>G
XM_011513724.1:c.1775A>G	XP_011512026.1:p.Gln592Arg
XM_011513725.1:c.1709A>G	XP_011512027.1:p.Gln570Arg
XM_011513725.2:c.1709A>G	XP_011512027.1:p.Gln570Arg
XM_011513726.1:c.1295A>G	XP_011512028.1:p.Gln432Arg
XM_011513726.3:c.1295A>G	XP_011512028.1:p.Gln432Arg
XM_011513727.1:c.1295A>G	XP_011512029.1:p.Gln432Arg
XM_011513728.1:c.1295A>G	XP_011512030.1:p.Gln432Arg
XM_011513729.1:c.1775A>G	XP_011512031.1:p.Gln592Arg
XM_017008501.1:c.1295A>G	XP_016863990.1:p.Gln432Arg
XR_001741306.1:n.1839A>G
XR_001741307.1:n.1839A>G
XR_001741308.1:n.1839A>G
XR_001741309.1:n.1839A>G
XR_001741310.1:n.1839A>G
XR_001741311.2:n.1688A>G
XR_001741312.1:n.1839A>G
XR_925155.1:n.1839A>G