Canonical Allele Identifier: CA2761116395

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275021_39275025del , CM000666.2:g.39275021_39275025del	GRCh38
NC_000004.11:g.39276641_39276645del , CM000666.1:g.39276641_39276645del	GRCh37
NC_000004.10:g.38953036_38953040del	NCBI36
NG_031813.1:g.97618_97622del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+63_3716+67del MANE Select	ENSP00000382717.3:n.3716+63_3716+67del
ENST00000399820.7:c.3716+63_3716+67del	ENSP00000382717.3:n.3716+63_3716+67del
ENST00000506869.5:c.*3297+63_*3297+67del	ENSP00000424319.1:n.*3297+63_*3297+67del
ENST00000512095.5:n.2777_2781del
ENST00000512534.5:n.2027+63_2027+67del
NM_025132.3:c.3716+63_3716+67del	NP_079408.3:n.3716+63_3716+67del
XM_011513724.1:c.3728+63_3728+67del	XP_011512026.1:n.3728+63_3728+67del
XM_011513725.1:c.3662+63_3662+67del	XP_011512027.1:n.3662+63_3662+67del
XM_011513726.1:c.3248+63_3248+67del	XP_011512028.1:n.3248+63_3248+67del
XM_011513727.1:c.3248+63_3248+67del	XP_011512029.1:n.3248+63_3248+67del
XM_011513728.1:c.3236+63_3236+67del	XP_011512030.1:n.3236+63_3236+67del
XR_925155.1:n.5426+63_5426+67del
NM_001317924.1:c.3236+63_3236+67del	NP_001304853.1:n.3236+63_3236+67del
XM_011513725.2:c.3662+63_3662+67del	XP_011512027.1:n.3662+63_3662+67del
XM_011513726.3:c.3248+63_3248+67del	XP_011512028.1:n.3248+63_3248+67del
XM_017008501.1:c.3236+63_3236+67del	XP_016863990.1:n.3236+63_3236+67del
XR_001741306.1:n.3792+63_3792+67del
XR_001741307.1:n.3780+63_3780+67del
XR_001741308.1:n.5426+63_5426+67del
XR_001741309.1:n.5414+63_5414+67del
XR_001741310.1:n.5414+63_5414+67del
XR_001741311.2:n.5263+63_5263+67del
NM_025132.4:c.3716+63_3716+67del MANE Select	NP_079408.3:n.3716+63_3716+67del
NM_001317924.2:c.3236+63_3236+67del	NP_001304853.1:n.3236+63_3236+67del