Canonical Allele Identifier: CA356633763

Gene: WDR19

Linked Data

• gnomAD v4: 4-39205170-G-T
• MyVariant Identifiers: chr4:g.39206790G>T (hg19) ; chr4:g.39205170G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205170G>T , CM000666.2:g.39205170G>T	GRCh38
NC_000004.11:g.39206790G>T , CM000666.1:g.39206790G>T	GRCh37
NC_000004.10:g.38883185G>T	NCBI36
NG_031813.1:g.27767G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.620G>T MANE Select	ENSP00000382717.3:p.Gly207Val
ENST00000399820.7:c.620G>T	ENSP00000382717.3:p.Gly207Val
ENST00000503697.5:c.*88G>T	ENSP00000423706.1:n.*88G>T
ENST00000505055.5:c.*201G>T	ENSP00000425949.1:n.*201G>T
ENST00000506503.1:c.620G>T	ENSP00000423491.1:p.Gly207Val
ENST00000506869.5:c.*201G>T	ENSP00000424319.1:n.*201G>T
ENST00000511729.5:n.40+22607G>T
ENST00000512448.1:n.214G>T
NM_025132.3:c.620G>T	NP_079408.3:p.Gly207Val
XM_011513724.1:c.620G>T	XP_011512026.1:p.Gly207Val
XM_011513725.1:c.554G>T	XP_011512027.1:p.Gly185Val
XM_011513726.1:c.140G>T	XP_011512028.1:p.Gly47Val
XM_011513727.1:c.140G>T	XP_011512029.1:p.Gly47Val
XM_011513728.1:c.140G>T	XP_011512030.1:p.Gly47Val
XM_011513729.1:c.620G>T	XP_011512031.1:p.Gly207Val
XR_925155.1:n.684G>T
NM_001317924.1:c.140G>T	NP_001304853.1:p.Gly47Val
XM_011513725.2:c.554G>T	XP_011512027.1:p.Gly185Val
XM_011513726.3:c.140G>T	XP_011512028.1:p.Gly47Val
XM_017008501.1:c.140G>T	XP_016863990.1:p.Gly47Val
XR_001741306.1:n.684G>T
XR_001741307.1:n.684G>T
XR_001741308.1:n.684G>T
XR_001741309.1:n.684G>T
XR_001741310.1:n.684G>T
XR_001741311.2:n.533G>T
XR_001741312.1:n.684G>T
NM_025132.4:c.620G>T MANE Select	NP_079408.3:p.Gly207Val
NM_001317924.2:c.140G>T	NP_001304853.1:p.Gly47Val