Canonical Allele Identifier: CA2761116370

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39274998_39275002del , CM000666.2:g.39274998_39275002del	GRCh38
NC_000004.11:g.39276618_39276622del , CM000666.1:g.39276618_39276622del	GRCh37
NC_000004.10:g.38953013_38953017del	NCBI36
NG_031813.1:g.97595_97599del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+40_3716+44del MANE Select	ENSP00000382717.3:n.3716+40_3716+44del
ENST00000399820.7:c.3716+40_3716+44del	ENSP00000382717.3:n.3716+40_3716+44del
ENST00000506869.5:c.*3297+40_*3297+44del	ENSP00000424319.1:n.*3297+40_*3297+44del
ENST00000512095.5:n.2754_2758del
ENST00000512534.5:n.2027+40_2027+44del
NM_025132.3:c.3716+40_3716+44del	NP_079408.3:n.3716+40_3716+44del
XM_011513724.1:c.3728+40_3728+44del	XP_011512026.1:n.3728+40_3728+44del
XM_011513725.1:c.3662+40_3662+44del	XP_011512027.1:n.3662+40_3662+44del
XM_011513726.1:c.3248+40_3248+44del	XP_011512028.1:n.3248+40_3248+44del
XM_011513727.1:c.3248+40_3248+44del	XP_011512029.1:n.3248+40_3248+44del
XM_011513728.1:c.3236+40_3236+44del	XP_011512030.1:n.3236+40_3236+44del
XR_925155.1:n.5426+40_5426+44del
NM_001317924.1:c.3236+40_3236+44del	NP_001304853.1:n.3236+40_3236+44del
XM_011513725.2:c.3662+40_3662+44del	XP_011512027.1:n.3662+40_3662+44del
XM_011513726.3:c.3248+40_3248+44del	XP_011512028.1:n.3248+40_3248+44del
XM_017008501.1:c.3236+40_3236+44del	XP_016863990.1:n.3236+40_3236+44del
XR_001741306.1:n.3792+40_3792+44del
XR_001741307.1:n.3780+40_3780+44del
XR_001741308.1:n.5426+40_5426+44del
XR_001741309.1:n.5414+40_5414+44del
XR_001741310.1:n.5414+40_5414+44del
XR_001741311.2:n.5263+40_5263+44del
NM_025132.4:c.3716+40_3716+44del MANE Select	NP_079408.3:n.3716+40_3716+44del
NM_001317924.2:c.3236+40_3236+44del	NP_001304853.1:n.3236+40_3236+44del