Canonical Allele Identifier: CA1451994361

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205291_39205292delinsAC , CM000666.2:g.39205291_39205292delinsAC	GRCh38
NC_000004.11:g.39206911_39206912delinsAC , CM000666.1:g.39206911_39206912delinsAC	GRCh37
NC_000004.10:g.38883306_38883307delinsAC	NCBI36
NG_031813.1:g.27888_27889delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.716+25_716+26delinsAC MANE Select	ENSP00000382717.3:n.716+25_716+26delinsAC
ENST00000399820.7:c.716+25_716+26delinsAC	ENSP00000382717.3:n.716+25_716+26delinsAC
ENST00000503697.5:c.*184+25_*184+26delinsAC	ENSP00000423706.1:n.*184+25_*184+26delinsAC
ENST00000505055.5:c.*297+25_*297+26delinsAC	ENSP00000425949.1:n.*297+25_*297+26delinsAC
ENST00000506503.1:c.716+25_716+26delinsAC	ENSP00000423491.1:n.716+25_716+26delinsAC
ENST00000506869.5:c.*297+25_*297+26delinsAC	ENSP00000424319.1:n.*297+25_*297+26delinsAC
ENST00000511729.5:n.40+22728_40+22729delinsAC
ENST00000512448.1:n.310+25_310+26delinsAC
NM_025132.3:c.716+25_716+26delinsAC	NP_079408.3:n.716+25_716+26delinsAC
XM_011513724.1:c.716+25_716+26delinsAC	XP_011512026.1:n.716+25_716+26delinsAC
XM_011513725.1:c.650+25_650+26delinsAC	XP_011512027.1:n.650+25_650+26delinsAC
XM_011513726.1:c.236+25_236+26delinsAC	XP_011512028.1:n.236+25_236+26delinsAC
XM_011513727.1:c.236+25_236+26delinsAC	XP_011512029.1:n.236+25_236+26delinsAC
XM_011513728.1:c.236+25_236+26delinsAC	XP_011512030.1:n.236+25_236+26delinsAC
XM_011513729.1:c.716+25_716+26delinsAC	XP_011512031.1:n.716+25_716+26delinsAC
XR_925155.1:n.780+25_780+26delinsAC
NM_001317924.1:c.236+25_236+26delinsAC	NP_001304853.1:n.236+25_236+26delinsAC
XM_011513725.2:c.650+25_650+26delinsAC	XP_011512027.1:n.650+25_650+26delinsAC
XM_011513726.3:c.236+25_236+26delinsAC	XP_011512028.1:n.236+25_236+26delinsAC
XM_017008501.1:c.236+25_236+26delinsAC	XP_016863990.1:n.236+25_236+26delinsAC
XR_001741306.1:n.780+25_780+26delinsAC
XR_001741307.1:n.780+25_780+26delinsAC
XR_001741308.1:n.780+25_780+26delinsAC
XR_001741309.1:n.780+25_780+26delinsAC
XR_001741310.1:n.780+25_780+26delinsAC
XR_001741311.2:n.629+25_629+26delinsAC
XR_001741312.1:n.780+25_780+26delinsAC
NM_025132.4:c.716+25_716+26delinsAC MANE Select	NP_079408.3:n.716+25_716+26delinsAC
NM_001317924.2:c.236+25_236+26delinsAC	NP_001304853.1:n.236+25_236+26delinsAC