Canonical Allele Identifier: CA1451994408

Gene: WDR19

Linked Data

• dbSNP Id: rs1727836840
• gnomAD v4: 4-39205362-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205362A>G , CM000666.2:g.39205362A>G	GRCh38
NC_000004.11:g.39206982A>G , CM000666.1:g.39206982A>G	GRCh37
NC_000004.10:g.38883377A>G	NCBI36
NG_031813.1:g.27959A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.716+96A>G MANE Select	ENSP00000382717.3:n.716+96A>G
ENST00000399820.7:c.716+96A>G	ENSP00000382717.3:n.716+96A>G
ENST00000503697.5:c.*184+96A>G	ENSP00000423706.1:n.*184+96A>G
ENST00000505055.5:c.*297+96A>G	ENSP00000425949.1:n.*297+96A>G
ENST00000506503.1:c.716+96A>G	ENSP00000423491.1:n.716+96A>G
ENST00000506869.5:c.*297+96A>G	ENSP00000424319.1:n.*297+96A>G
ENST00000511729.5:n.40+22799A>G
ENST00000512448.1:n.310+96A>G
NM_025132.3:c.716+96A>G	NP_079408.3:n.716+96A>G
XM_011513724.1:c.716+96A>G	XP_011512026.1:n.716+96A>G
XM_011513725.1:c.650+96A>G	XP_011512027.1:n.650+96A>G
XM_011513726.1:c.236+96A>G	XP_011512028.1:n.236+96A>G
XM_011513727.1:c.236+96A>G	XP_011512029.1:n.236+96A>G
XM_011513728.1:c.236+96A>G	XP_011512030.1:n.236+96A>G
XM_011513729.1:c.716+96A>G	XP_011512031.1:n.716+96A>G
XR_925155.1:n.780+96A>G
NM_001317924.1:c.236+96A>G	NP_001304853.1:n.236+96A>G
XM_011513725.2:c.650+96A>G	XP_011512027.1:n.650+96A>G
XM_011513726.3:c.236+96A>G	XP_011512028.1:n.236+96A>G
XM_017008501.1:c.236+96A>G	XP_016863990.1:n.236+96A>G
XR_001741306.1:n.780+96A>G
XR_001741307.1:n.780+96A>G
XR_001741308.1:n.780+96A>G
XR_001741309.1:n.780+96A>G
XR_001741310.1:n.780+96A>G
XR_001741311.2:n.629+96A>G
XR_001741312.1:n.780+96A>G
NM_025132.4:c.716+96A>G MANE Select	NP_079408.3:n.716+96A>G
NM_001317924.2:c.236+96A>G	NP_001304853.1:n.236+96A>G