Canonical Allele Identifier: CA2573137747

Gene: WDR19

Linked Data

• ClinVar Variation Id: 1614775
• ClinVar RCV Id: RCV002073952
• dbSNP Id: rs2109406442

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244457T>G , CM000666.2:g.39244457T>G	GRCh38
NC_000004.11:g.39246077T>G , CM000666.1:g.39246077T>G	GRCh37
NC_000004.10:g.38922472T>G	NCBI36
NG_031813.1:g.67054T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2563-13T>G MANE Select	ENSP00000382717.3:n.2563-13T>G
ENST00000399820.7:c.2563-13T>G	ENSP00000382717.3:n.2563-13T>G
ENST00000506869.5:c.*2144-13T>G	ENSP00000424319.1:n.*2144-13T>G
ENST00000512095.5:n.1561-13T>G
NM_025132.3:c.2563-13T>G	NP_079408.3:n.2563-13T>G
XM_011513724.1:c.2575-13T>G	XP_011512026.1:n.2575-13T>G
XM_011513725.1:c.2509-13T>G	XP_011512027.1:n.2509-13T>G
XM_011513726.1:c.2095-13T>G	XP_011512028.1:n.2095-13T>G
XM_011513727.1:c.2095-13T>G	XP_011512029.1:n.2095-13T>G
XM_011513728.1:c.2083-13T>G	XP_011512030.1:n.2083-13T>G
XM_011513729.1:c.2575-13T>G	XP_011512031.1:n.2575-13T>G
XR_925155.1:n.2639-13T>G
NM_001317924.1:c.2083-13T>G	NP_001304853.1:n.2083-13T>G
XM_011513725.2:c.2509-13T>G	XP_011512027.1:n.2509-13T>G
XM_011513726.3:c.2095-13T>G	XP_011512028.1:n.2095-13T>G
XM_017008501.1:c.2083-13T>G	XP_016863990.1:n.2083-13T>G
XR_001741306.1:n.2639-13T>G
XR_001741307.1:n.2627-13T>G
XR_001741308.1:n.2639-13T>G
XR_001741309.1:n.2627-13T>G
XR_001741310.1:n.2627-13T>G
XR_001741311.2:n.2476-13T>G
NM_025132.4:c.2563-13T>G MANE Select	NP_079408.3:n.2563-13T>G
NM_001317924.2:c.2083-13T>G	NP_001304853.1:n.2083-13T>G