Canonical Allele Identifier: CA438939441

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39207324T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205704T>G , CM000666.2:g.39205704T>G	GRCh38
NC_000004.11:g.39207324T>G , CM000666.1:g.39207324T>G	GRCh37
NC_000004.10:g.38883719T>G	NCBI36
NG_031813.1:g.28301T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.858T>G MANE Select	ENSP00000382717.3:p.Thr286=
ENST00000399820.7:c.858T>G	ENSP00000382717.3:p.Thr286=
ENST00000503697.5:c.*326T>G	ENSP00000423706.1:n.*326T>G
ENST00000506503.1:c.858T>G	ENSP00000423491.1:p.Thr286=
ENST00000506869.5:c.*439T>G	ENSP00000424319.1:n.*439T>G
ENST00000511729.5:n.41-22854T>G
ENST00000512448.1:n.452T>G
NM_025132.3:c.858T>G	NP_079408.3:p.Thr286=
XM_011513724.1:c.858T>G	XP_011512026.1:p.Thr286=
XM_011513725.1:c.792T>G	XP_011512027.1:p.Thr264=
XM_011513726.1:c.378T>G	XP_011512028.1:p.Thr126=
XM_011513727.1:c.378T>G	XP_011512029.1:p.Thr126=
XM_011513728.1:c.378T>G	XP_011512030.1:p.Thr126=
XM_011513729.1:c.858T>G	XP_011512031.1:p.Thr286=
XR_925155.1:n.922T>G
NM_001317924.1:c.378T>G	NP_001304853.1:p.Thr126=
XM_011513725.2:c.792T>G	XP_011512027.1:p.Thr264=
XM_011513726.3:c.378T>G	XP_011512028.1:p.Thr126=
XM_017008501.1:c.378T>G	XP_016863990.1:p.Thr126=
XR_001741306.1:n.922T>G
XR_001741307.1:n.922T>G
XR_001741308.1:n.922T>G
XR_001741309.1:n.922T>G
XR_001741310.1:n.922T>G
XR_001741311.2:n.771T>G
XR_001741312.1:n.922T>G
NM_025132.4:c.858T>G MANE Select	NP_079408.3:p.Thr286=
NM_001317924.2:c.378T>G	NP_001304853.1:p.Thr126=