Canonical Allele Identifier: CA2761116360

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39274995_39274999del , CM000666.2:g.39274995_39274999del	GRCh38
NC_000004.11:g.39276615_39276619del , CM000666.1:g.39276615_39276619del	GRCh37
NC_000004.10:g.38953010_38953014del	NCBI36
NG_031813.1:g.97592_97596del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+37_3716+41del MANE Select	ENSP00000382717.3:n.3716+37_3716+41del
ENST00000399820.7:c.3716+37_3716+41del	ENSP00000382717.3:n.3716+37_3716+41del
ENST00000506869.5:c.*3297+37_*3297+41del	ENSP00000424319.1:n.*3297+37_*3297+41del
ENST00000512095.5:n.2751_2755del
ENST00000512534.5:n.2027+37_2027+41del
NM_025132.3:c.3716+37_3716+41del	NP_079408.3:n.3716+37_3716+41del
XM_011513724.1:c.3728+37_3728+41del	XP_011512026.1:n.3728+37_3728+41del
XM_011513725.1:c.3662+37_3662+41del	XP_011512027.1:n.3662+37_3662+41del
XM_011513726.1:c.3248+37_3248+41del	XP_011512028.1:n.3248+37_3248+41del
XM_011513727.1:c.3248+37_3248+41del	XP_011512029.1:n.3248+37_3248+41del
XM_011513728.1:c.3236+37_3236+41del	XP_011512030.1:n.3236+37_3236+41del
XR_925155.1:n.5426+37_5426+41del
NM_001317924.1:c.3236+37_3236+41del	NP_001304853.1:n.3236+37_3236+41del
XM_011513725.2:c.3662+37_3662+41del	XP_011512027.1:n.3662+37_3662+41del
XM_011513726.3:c.3248+37_3248+41del	XP_011512028.1:n.3248+37_3248+41del
XM_017008501.1:c.3236+37_3236+41del	XP_016863990.1:n.3236+37_3236+41del
XR_001741306.1:n.3792+37_3792+41del
XR_001741307.1:n.3780+37_3780+41del
XR_001741308.1:n.5426+37_5426+41del
XR_001741309.1:n.5414+37_5414+41del
XR_001741310.1:n.5414+37_5414+41del
XR_001741311.2:n.5263+37_5263+41del
NM_025132.4:c.3716+37_3716+41del MANE Select	NP_079408.3:n.3716+37_3716+41del
NM_001317924.2:c.3236+37_3236+41del	NP_001304853.1:n.3236+37_3236+41del