Canonical Allele Identifier: CA2670356344

Gene: WDR19

Linked Data

• gnomAD v4: 4-39205707-TAAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205710_39205712del , CM000666.2:g.39205710_39205712del	GRCh38
NC_000004.11:g.39207330_39207332del , CM000666.1:g.39207330_39207332del	GRCh37
NC_000004.10:g.38883725_38883727del	NCBI36
NG_031813.1:g.28307_28309del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.864_866del MANE Select	ENSP00000382717.3:p.Asn288del
ENST00000399820.7:c.864_866del	ENSP00000382717.3:p.Asn288del
ENST00000503697.5:c.*332_*334del	ENSP00000423706.1:n.*332_*334del
ENST00000506503.1:c.864_866del	ENSP00000423491.1:p.Asn288del
ENST00000506869.5:c.*445_*447del	ENSP00000424319.1:n.*445_*447del
ENST00000511729.5:n.41-22848_41-22846del
ENST00000512448.1:n.458_460del
NM_025132.3:c.864_866del	NP_079408.3:p.Asn288del
XM_011513724.1:c.864_866del	XP_011512026.1:p.Asn288del
XM_011513725.1:c.798_800del	XP_011512027.1:p.Asn266del
XM_011513726.1:c.384_386del	XP_011512028.1:p.Asn128del
XM_011513727.1:c.384_386del	XP_011512029.1:p.Asn128del
XM_011513728.1:c.384_386del	XP_011512030.1:p.Asn128del
XM_011513729.1:c.864_866del	XP_011512031.1:p.Asn288del
XR_925155.1:n.928_930del
NM_001317924.1:c.384_386del	NP_001304853.1:p.Asn128del
XM_011513725.2:c.798_800del	XP_011512027.1:p.Asn266del
XM_011513726.3:c.384_386del	XP_011512028.1:p.Asn128del
XM_017008501.1:c.384_386del	XP_016863990.1:p.Asn128del
XR_001741306.1:n.928_930del
XR_001741307.1:n.928_930del
XR_001741308.1:n.928_930del
XR_001741309.1:n.928_930del
XR_001741310.1:n.928_930del
XR_001741311.2:n.777_779del
XR_001741312.1:n.928_930del
NM_025132.4:c.864_866del MANE Select	NP_079408.3:p.Asn288del
NM_001317924.2:c.384_386del	NP_001304853.1:p.Asn128del