Canonical Allele Identifier: CA2670362617

Gene: WDR19

Linked Data

• gnomAD v4: 4-39275211-A-ACG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275212_39275213insGC , CM000666.2:g.39275212_39275213insGC	GRCh38
NC_000004.11:g.39276832_39276833insGC , CM000666.1:g.39276832_39276833insGC	GRCh37
NC_000004.10:g.38953227_38953228insGC	NCBI36
NG_031813.1:g.97809_97810insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+254_3716+255insGC MANE Select	ENSP00000382717.3:n.3716+254_3716+255insGC
ENST00000399820.7:c.3716+254_3716+255insGC	ENSP00000382717.3:n.3716+254_3716+255insGC
ENST00000506869.5:c.*3297+254_*3297+255insGC	ENSP00000424319.1:n.*3297+254_*3297+255insGC
ENST00000512095.5:n.2968_2969insGC
ENST00000512534.5:n.2027+254_2027+255insGC
NM_025132.3:c.3716+254_3716+255insGC	NP_079408.3:n.3716+254_3716+255insGC
XM_011513724.1:c.3728+254_3728+255insGC	XP_011512026.1:n.3728+254_3728+255insGC
XM_011513725.1:c.3662+254_3662+255insGC	XP_011512027.1:n.3662+254_3662+255insGC
XM_011513726.1:c.3248+254_3248+255insGC	XP_011512028.1:n.3248+254_3248+255insGC
XM_011513727.1:c.3248+254_3248+255insGC	XP_011512029.1:n.3248+254_3248+255insGC
XM_011513728.1:c.3236+254_3236+255insGC	XP_011512030.1:n.3236+254_3236+255insGC
XR_925155.1:n.5426+254_5426+255insGC
NM_001317924.1:c.3236+254_3236+255insGC	NP_001304853.1:n.3236+254_3236+255insGC
XM_011513725.2:c.3662+254_3662+255insGC	XP_011512027.1:n.3662+254_3662+255insGC
XM_011513726.3:c.3248+254_3248+255insGC	XP_011512028.1:n.3248+254_3248+255insGC
XM_017008501.1:c.3236+254_3236+255insGC	XP_016863990.1:n.3236+254_3236+255insGC
XR_001741306.1:n.3792+254_3792+255insGC
XR_001741307.1:n.3780+254_3780+255insGC
XR_001741308.1:n.5426+254_5426+255insGC
XR_001741309.1:n.5414+254_5414+255insGC
XR_001741310.1:n.5414+254_5414+255insGC
XR_001741311.2:n.5263+254_5263+255insGC
NM_025132.4:c.3716+254_3716+255insGC MANE Select	NP_079408.3:n.3716+254_3716+255insGC
NM_001317924.2:c.3236+254_3236+255insGC	NP_001304853.1:n.3236+254_3236+255insGC