Canonical Allele Identifier: CA2573137689

Gene: WDR19

Linked Data

• ClinVar Variation Id: 1566142
• ClinVar RCV Id: RCV002207270
• dbSNP Id: rs2109299804

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205134C>G , CM000666.2:g.39205134C>G	GRCh38
NC_000004.11:g.39206754C>G , CM000666.1:g.39206754C>G	GRCh37
NC_000004.10:g.38883149C>G	NCBI36
NG_031813.1:g.27731C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.604-20C>G MANE Select	ENSP00000382717.3:n.604-20C>G
ENST00000399820.7:c.604-20C>G	ENSP00000382717.3:n.604-20C>G
ENST00000503697.5:c.*72-20C>G	ENSP00000423706.1:n.*72-20C>G
ENST00000505055.5:c.*185-20C>G	ENSP00000425949.1:n.*185-20C>G
ENST00000506503.1:c.604-20C>G	ENSP00000423491.1:n.604-20C>G
ENST00000506869.5:c.*185-20C>G	ENSP00000424319.1:n.*185-20C>G
ENST00000511729.5:n.40+22571C>G
ENST00000512448.1:n.198-20C>G
NM_025132.3:c.604-20C>G	NP_079408.3:n.604-20C>G
XM_011513724.1:c.604-20C>G	XP_011512026.1:n.604-20C>G
XM_011513725.1:c.538-20C>G	XP_011512027.1:n.538-20C>G
XM_011513726.1:c.124-20C>G	XP_011512028.1:n.124-20C>G
XM_011513727.1:c.124-20C>G	XP_011512029.1:n.124-20C>G
XM_011513728.1:c.124-20C>G	XP_011512030.1:n.124-20C>G
XM_011513729.1:c.604-20C>G	XP_011512031.1:n.604-20C>G
XR_925155.1:n.668-20C>G
NM_001317924.1:c.124-20C>G	NP_001304853.1:n.124-20C>G
XM_011513725.2:c.538-20C>G	XP_011512027.1:n.538-20C>G
XM_011513726.3:c.124-20C>G	XP_011512028.1:n.124-20C>G
XM_017008501.1:c.124-20C>G	XP_016863990.1:n.124-20C>G
XR_001741306.1:n.668-20C>G
XR_001741307.1:n.668-20C>G
XR_001741308.1:n.668-20C>G
XR_001741309.1:n.668-20C>G
XR_001741310.1:n.668-20C>G
XR_001741311.2:n.517-20C>G
XR_001741312.1:n.668-20C>G
NM_025132.4:c.604-20C>G MANE Select	NP_079408.3:n.604-20C>G
NM_001317924.2:c.124-20C>G	NP_001304853.1:n.124-20C>G