Canonical Allele Identifier: CA2761116401

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275024_39275025del , CM000666.2:g.39275024_39275025del	GRCh38
NC_000004.11:g.39276644_39276645del , CM000666.1:g.39276644_39276645del	GRCh37
NC_000004.10:g.38953039_38953040del	NCBI36
NG_031813.1:g.97621_97622del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+66_3716+67del MANE Select	ENSP00000382717.3:n.3716+66_3716+67del
ENST00000399820.7:c.3716+66_3716+67del	ENSP00000382717.3:n.3716+66_3716+67del
ENST00000506869.5:c.*3297+66_*3297+67del	ENSP00000424319.1:n.*3297+66_*3297+67del
ENST00000512095.5:n.2780_2781del
ENST00000512534.5:n.2027+66_2027+67del
NM_025132.3:c.3716+66_3716+67del	NP_079408.3:n.3716+66_3716+67del
XM_011513724.1:c.3728+66_3728+67del	XP_011512026.1:n.3728+66_3728+67del
XM_011513725.1:c.3662+66_3662+67del	XP_011512027.1:n.3662+66_3662+67del
XM_011513726.1:c.3248+66_3248+67del	XP_011512028.1:n.3248+66_3248+67del
XM_011513727.1:c.3248+66_3248+67del	XP_011512029.1:n.3248+66_3248+67del
XM_011513728.1:c.3236+66_3236+67del	XP_011512030.1:n.3236+66_3236+67del
XR_925155.1:n.5426+66_5426+67del
NM_001317924.1:c.3236+66_3236+67del	NP_001304853.1:n.3236+66_3236+67del
XM_011513725.2:c.3662+66_3662+67del	XP_011512027.1:n.3662+66_3662+67del
XM_011513726.3:c.3248+66_3248+67del	XP_011512028.1:n.3248+66_3248+67del
XM_017008501.1:c.3236+66_3236+67del	XP_016863990.1:n.3236+66_3236+67del
XR_001741306.1:n.3792+66_3792+67del
XR_001741307.1:n.3780+66_3780+67del
XR_001741308.1:n.5426+66_5426+67del
XR_001741309.1:n.5414+66_5414+67del
XR_001741310.1:n.5414+66_5414+67del
XR_001741311.2:n.5263+66_5263+67del
NM_025132.4:c.3716+66_3716+67del MANE Select	NP_079408.3:n.3716+66_3716+67del
NM_001317924.2:c.3236+66_3236+67del	NP_001304853.1:n.3236+66_3236+67del