Canonical Allele Identifier: CA356638419

Gene: WDR19

Linked Data

• ClinVar Variation Id: 2090526
• ClinVar RCV Id: RCV003013147
• MyVariant Identifiers: chr4:g.39246116T>G (hg19) ; chr4:g.39244496T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244496T>G , CM000666.2:g.39244496T>G	GRCh38
NC_000004.11:g.39246116T>G , CM000666.1:g.39246116T>G	GRCh37
NC_000004.10:g.38922511T>G	NCBI36
NG_031813.1:g.67093T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2589T>G MANE Select	ENSP00000382717.3:p.Tyr863Ter
ENST00000399820.7:c.2589T>G	ENSP00000382717.3:p.Tyr863Ter
ENST00000506869.5:c.*2170T>G	ENSP00000424319.1:n.*2170T>G
ENST00000512095.5:n.1587T>G
NM_025132.3:c.2589T>G	NP_079408.3:p.Tyr863Ter
XM_011513724.1:c.2601T>G	XP_011512026.1:p.Tyr867Ter
XM_011513725.1:c.2535T>G	XP_011512027.1:p.Tyr845Ter
XM_011513726.1:c.2121T>G	XP_011512028.1:p.Tyr707Ter
XM_011513727.1:c.2121T>G	XP_011512029.1:p.Tyr707Ter
XM_011513728.1:c.2109T>G	XP_011512030.1:p.Tyr703Ter
XM_011513729.1:c.2601T>G	XP_011512031.1:p.Tyr867Ter
XR_925155.1:n.2665T>G
NM_001317924.1:c.2109T>G	NP_001304853.1:p.Tyr703Ter
XM_011513725.2:c.2535T>G	XP_011512027.1:p.Tyr845Ter
XM_011513726.3:c.2121T>G	XP_011512028.1:p.Tyr707Ter
XM_017008501.1:c.2109T>G	XP_016863990.1:p.Tyr703Ter
XR_001741306.1:n.2665T>G
XR_001741307.1:n.2653T>G
XR_001741308.1:n.2665T>G
XR_001741309.1:n.2653T>G
XR_001741310.1:n.2653T>G
XR_001741311.2:n.2502T>G
NM_025132.4:c.2589T>G MANE Select	NP_079408.3:p.Tyr863Ter
NM_001317924.2:c.2109T>G	NP_001304853.1:p.Tyr703Ter