Canonical Allele Identifier: CA1451994240

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205183_39205184delinsGT , CM000666.2:g.39205183_39205184delinsGT	GRCh38
NC_000004.11:g.39206803_39206804delinsGT , CM000666.1:g.39206803_39206804delinsGT	GRCh37
NC_000004.10:g.38883198_38883199delinsGT	NCBI36
NG_031813.1:g.27780_27781delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.633_634delinsGT MANE Select	ENSP00000382717.3:p.Leu211=
ENST00000399820.7:c.633_634delinsGT	ENSP00000382717.3:p.Leu211=
ENST00000503697.5:c.*101_*102delinsGT	ENSP00000423706.1:n.*101_*102delinsGT
ENST00000505055.5:c.*214_*215delinsGT	ENSP00000425949.1:n.*214_*215delinsGT
ENST00000506503.1:c.633_634delinsGT	ENSP00000423491.1:p.Leu211=
ENST00000506869.5:c.*214_*215delinsGT	ENSP00000424319.1:n.*214_*215delinsGT
ENST00000511729.5:n.40+22620_40+22621delinsGT
ENST00000512448.1:n.227_228delinsGT
NM_025132.3:c.633_634delinsGT	NP_079408.3:p.Leu211=
XM_011513724.1:c.633_634delinsGT	XP_011512026.1:p.Leu211=
XM_011513725.1:c.567_568delinsGT	XP_011512027.1:p.Leu189=
XM_011513726.1:c.153_154delinsGT	XP_011512028.1:p.Leu51=
XM_011513727.1:c.153_154delinsGT	XP_011512029.1:p.Leu51=
XM_011513728.1:c.153_154delinsGT	XP_011512030.1:p.Leu51=
XM_011513729.1:c.633_634delinsGT	XP_011512031.1:p.Leu211=
XR_925155.1:n.697_698delinsGT
NM_001317924.1:c.153_154delinsGT	NP_001304853.1:p.Leu51=
XM_011513725.2:c.567_568delinsGT	XP_011512027.1:p.Leu189=
XM_011513726.3:c.153_154delinsGT	XP_011512028.1:p.Leu51=
XM_017008501.1:c.153_154delinsGT	XP_016863990.1:p.Leu51=
XR_001741306.1:n.697_698delinsGT
XR_001741307.1:n.697_698delinsGT
XR_001741308.1:n.697_698delinsGT
XR_001741309.1:n.697_698delinsGT
XR_001741310.1:n.697_698delinsGT
XR_001741311.2:n.546_547delinsGT
XR_001741312.1:n.697_698delinsGT
NM_025132.4:c.633_634delinsGT MANE Select	NP_079408.3:p.Leu211=
NM_001317924.2:c.153_154delinsGT	NP_001304853.1:p.Leu51=