Canonical Allele Identifier: CA2761116409

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275029_39275030insACA , CM000666.2:g.39275029_39275030insACA	GRCh38
NC_000004.11:g.39276649_39276650insACA , CM000666.1:g.39276649_39276650insACA	GRCh37
NC_000004.10:g.38953044_38953045insACA	NCBI36
NG_031813.1:g.97626_97627insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+71_3716+72insACA MANE Select	ENSP00000382717.3:n.3716+71_3716+72insACA
ENST00000399820.7:c.3716+71_3716+72insACA	ENSP00000382717.3:n.3716+71_3716+72insACA
ENST00000506869.5:c.*3297+71_*3297+72insACA	ENSP00000424319.1:n.*3297+71_*3297+72insACA
ENST00000512095.5:n.2785_2786insACA
ENST00000512534.5:n.2027+71_2027+72insACA
NM_025132.3:c.3716+71_3716+72insACA	NP_079408.3:n.3716+71_3716+72insACA
XM_011513724.1:c.3728+71_3728+72insACA	XP_011512026.1:n.3728+71_3728+72insACA
XM_011513725.1:c.3662+71_3662+72insACA	XP_011512027.1:n.3662+71_3662+72insACA
XM_011513726.1:c.3248+71_3248+72insACA	XP_011512028.1:n.3248+71_3248+72insACA
XM_011513727.1:c.3248+71_3248+72insACA	XP_011512029.1:n.3248+71_3248+72insACA
XM_011513728.1:c.3236+71_3236+72insACA	XP_011512030.1:n.3236+71_3236+72insACA
XR_925155.1:n.5426+71_5426+72insACA
NM_001317924.1:c.3236+71_3236+72insACA	NP_001304853.1:n.3236+71_3236+72insACA
XM_011513725.2:c.3662+71_3662+72insACA	XP_011512027.1:n.3662+71_3662+72insACA
XM_011513726.3:c.3248+71_3248+72insACA	XP_011512028.1:n.3248+71_3248+72insACA
XM_017008501.1:c.3236+71_3236+72insACA	XP_016863990.1:n.3236+71_3236+72insACA
XR_001741306.1:n.3792+71_3792+72insACA
XR_001741307.1:n.3780+71_3780+72insACA
XR_001741308.1:n.5426+71_5426+72insACA
XR_001741309.1:n.5414+71_5414+72insACA
XR_001741310.1:n.5414+71_5414+72insACA
XR_001741311.2:n.5263+71_5263+72insACA
NM_025132.4:c.3716+71_3716+72insACA MANE Select	NP_079408.3:n.3716+71_3716+72insACA
NM_001317924.2:c.3236+71_3236+72insACA	NP_001304853.1:n.3236+71_3236+72insACA