Canonical Allele Identifier: CA2761116306

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39274973_39274974insACA , CM000666.2:g.39274973_39274974insACA	GRCh38
NC_000004.11:g.39276593_39276594insACA , CM000666.1:g.39276593_39276594insACA	GRCh37
NC_000004.10:g.38952988_38952989insACA	NCBI36
NG_031813.1:g.97570_97571insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+15_3716+16insACA MANE Select	ENSP00000382717.3:n.3716+15_3716+16insACA
ENST00000399820.7:c.3716+15_3716+16insACA	ENSP00000382717.3:n.3716+15_3716+16insACA
ENST00000506869.5:c.*3297+15_*3297+16insACA	ENSP00000424319.1:n.*3297+15_*3297+16insACA
ENST00000512095.5:n.2729_2730insACA
ENST00000512534.5:n.2027+15_2027+16insACA
NM_025132.3:c.3716+15_3716+16insACA	NP_079408.3:n.3716+15_3716+16insACA
XM_011513724.1:c.3728+15_3728+16insACA	XP_011512026.1:n.3728+15_3728+16insACA
XM_011513725.1:c.3662+15_3662+16insACA	XP_011512027.1:n.3662+15_3662+16insACA
XM_011513726.1:c.3248+15_3248+16insACA	XP_011512028.1:n.3248+15_3248+16insACA
XM_011513727.1:c.3248+15_3248+16insACA	XP_011512029.1:n.3248+15_3248+16insACA
XM_011513728.1:c.3236+15_3236+16insACA	XP_011512030.1:n.3236+15_3236+16insACA
XR_925155.1:n.5426+15_5426+16insACA
NM_001317924.1:c.3236+15_3236+16insACA	NP_001304853.1:n.3236+15_3236+16insACA
XM_011513725.2:c.3662+15_3662+16insACA	XP_011512027.1:n.3662+15_3662+16insACA
XM_011513726.3:c.3248+15_3248+16insACA	XP_011512028.1:n.3248+15_3248+16insACA
XM_017008501.1:c.3236+15_3236+16insACA	XP_016863990.1:n.3236+15_3236+16insACA
XR_001741306.1:n.3792+15_3792+16insACA
XR_001741307.1:n.3780+15_3780+16insACA
XR_001741308.1:n.5426+15_5426+16insACA
XR_001741309.1:n.5414+15_5414+16insACA
XR_001741310.1:n.5414+15_5414+16insACA
XR_001741311.2:n.5263+15_5263+16insACA
NM_025132.4:c.3716+15_3716+16insACA MANE Select	NP_079408.3:n.3716+15_3716+16insACA
NM_001317924.2:c.3236+15_3236+16insACA	NP_001304853.1:n.3236+15_3236+16insACA