Canonical Allele Identifier: CA2670362614

Gene: WDR19

Linked Data

• gnomAD v4: 4-39275209-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275213_39275214del , CM000666.2:g.39275213_39275214del	GRCh38
NC_000004.11:g.39276833_39276834del , CM000666.1:g.39276833_39276834del	GRCh37
NC_000004.10:g.38953228_38953229del	NCBI36
NG_031813.1:g.97810_97811del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+255_3716+256del MANE Select	ENSP00000382717.3:n.3716+255_3716+256del
ENST00000399820.7:c.3716+255_3716+256del	ENSP00000382717.3:n.3716+255_3716+256del
ENST00000506869.5:c.*3297+255_*3297+256del	ENSP00000424319.1:n.*3297+255_*3297+256del
ENST00000512095.5:n.2969_2970del
ENST00000512534.5:n.2027+255_2027+256del
NM_025132.3:c.3716+255_3716+256del	NP_079408.3:n.3716+255_3716+256del
XM_011513724.1:c.3728+255_3728+256del	XP_011512026.1:n.3728+255_3728+256del
XM_011513725.1:c.3662+255_3662+256del	XP_011512027.1:n.3662+255_3662+256del
XM_011513726.1:c.3248+255_3248+256del	XP_011512028.1:n.3248+255_3248+256del
XM_011513727.1:c.3248+255_3248+256del	XP_011512029.1:n.3248+255_3248+256del
XM_011513728.1:c.3236+255_3236+256del	XP_011512030.1:n.3236+255_3236+256del
XR_925155.1:n.5426+255_5426+256del
NM_001317924.1:c.3236+255_3236+256del	NP_001304853.1:n.3236+255_3236+256del
XM_011513725.2:c.3662+255_3662+256del	XP_011512027.1:n.3662+255_3662+256del
XM_011513726.3:c.3248+255_3248+256del	XP_011512028.1:n.3248+255_3248+256del
XM_017008501.1:c.3236+255_3236+256del	XP_016863990.1:n.3236+255_3236+256del
XR_001741306.1:n.3792+255_3792+256del
XR_001741307.1:n.3780+255_3780+256del
XR_001741308.1:n.5426+255_5426+256del
XR_001741309.1:n.5414+255_5414+256del
XR_001741310.1:n.5414+255_5414+256del
XR_001741311.2:n.5263+255_5263+256del
NM_025132.4:c.3716+255_3716+256del MANE Select	NP_079408.3:n.3716+255_3716+256del
NM_001317924.2:c.3236+255_3236+256del	NP_001304853.1:n.3236+255_3236+256del