Canonical Allele Identifier: CA2891833

Gene: WDR19

Linked Data

• ClinVar Variation Id: 348735
• ClinVar RCV Id: RCV000270771 ; RCV000955100 ; RCV000365336 ; RCV004530411
• dbSNP Id: rs377101599
• ExAC: 4:39219596 G / A
• gnomAD v2: 4-39219596-G-A
• gnomAD v3: 4-39217976-G-A
• gnomAD v4: 4-39217976-G-A
• MyVariant Identifiers: chr4:g.39219596G>A (hg19) ; chr4:g.39217976G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39217976G>A , CM000666.2:g.39217976G>A	GRCh38
NC_000004.11:g.39219596G>A , CM000666.1:g.39219596G>A	GRCh37
NC_000004.10:g.38895991G>A	NCBI36
NG_031813.1:g.40573G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.1357-7G>A MANE Select	ENSP00000382717.3:n.1357-7G>A
ENST00000399820.7:c.1357-7G>A	ENSP00000382717.3:n.1357-7G>A
ENST00000506503.1:c.1357-11G>A	ENSP00000423491.1:n.1357-11G>A
ENST00000506869.5:c.*938-7G>A	ENSP00000424319.1:n.*938-7G>A
ENST00000511729.5:n.41-10582G>A
ENST00000512095.5:n.355-7G>A
NM_025132.3:c.1357-7G>A	NP_079408.3:n.1357-7G>A
XM_011513724.1:c.1357-7G>A	XP_011512026.1:n.1357-7G>A
XM_011513725.1:c.1291-7G>A	XP_011512027.1:n.1291-7G>A
XM_011513726.1:c.877-7G>A	XP_011512028.1:n.877-7G>A
XM_011513727.1:c.877-7G>A	XP_011512029.1:n.877-7G>A
XM_011513728.1:c.877-7G>A	XP_011512030.1:n.877-7G>A
XM_011513729.1:c.1357-7G>A	XP_011512031.1:n.1357-7G>A
XR_925155.1:n.1421-7G>A
NM_001317924.1:c.877-7G>A	NP_001304853.1:n.877-7G>A
XM_011513725.2:c.1291-7G>A	XP_011512027.1:n.1291-7G>A
XM_011513726.3:c.877-7G>A	XP_011512028.1:n.877-7G>A
XM_017008501.1:c.877-7G>A	XP_016863990.1:n.877-7G>A
XR_001741306.1:n.1421-7G>A
XR_001741307.1:n.1421-7G>A
XR_001741308.1:n.1421-7G>A
XR_001741309.1:n.1421-7G>A
XR_001741310.1:n.1421-7G>A
XR_001741311.2:n.1270-7G>A
XR_001741312.1:n.1421-7G>A
NM_025132.4:c.1357-7G>A MANE Select	NP_079408.3:n.1357-7G>A
NM_001317924.2:c.877-7G>A	NP_001304853.1:n.877-7G>A