Canonical Allele Identifier: CA2761116126

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273124_39273125insACA , CM000666.2:g.39273124_39273125insACA	GRCh38
NC_000004.11:g.39274744_39274745insACA , CM000666.1:g.39274744_39274745insACA	GRCh37
NC_000004.10:g.38951139_38951140insACA	NCBI36
NG_031813.1:g.95721_95722insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3565+63_3565+64insACA MANE Select	ENSP00000382717.3:n.3565+63_3565+64insACA
ENST00000399820.7:c.3565+63_3565+64insACA	ENSP00000382717.3:n.3565+63_3565+64insACA
ENST00000506869.5:c.*3146+63_*3146+64insACA	ENSP00000424319.1:n.*3146+63_*3146+64insACA
ENST00000512095.5:n.2563+63_2563+64insACA
ENST00000512534.5:n.193_194insACA
NM_025132.3:c.3565+63_3565+64insACA	NP_079408.3:n.3565+63_3565+64insACA
XM_011513724.1:c.3577+63_3577+64insACA	XP_011512026.1:n.3577+63_3577+64insACA
XM_011513725.1:c.3511+63_3511+64insACA	XP_011512027.1:n.3511+63_3511+64insACA
XM_011513726.1:c.3097+63_3097+64insACA	XP_011512028.1:n.3097+63_3097+64insACA
XM_011513727.1:c.3097+63_3097+64insACA	XP_011512029.1:n.3097+63_3097+64insACA
XM_011513728.1:c.3085+63_3085+64insACA	XP_011512030.1:n.3085+63_3085+64insACA
XR_925155.1:n.3642-50_3642-49insACA
NM_001317924.1:c.3085+63_3085+64insACA	NP_001304853.1:n.3085+63_3085+64insACA
XM_011513725.2:c.3511+63_3511+64insACA	XP_011512027.1:n.3511+63_3511+64insACA
XM_011513726.3:c.3097+63_3097+64insACA	XP_011512028.1:n.3097+63_3097+64insACA
XM_017008501.1:c.3085+63_3085+64insACA	XP_016863990.1:n.3085+63_3085+64insACA
XR_001741306.1:n.3641+63_3641+64insACA
XR_001741307.1:n.3629+63_3629+64insACA
XR_001741308.1:n.3642-50_3642-49insACA
XR_001741309.1:n.3630-50_3630-49insACA
XR_001741310.1:n.3630-50_3630-49insACA
XR_001741311.2:n.3479-50_3479-49insACA
NM_025132.4:c.3565+63_3565+64insACA MANE Select	NP_079408.3:n.3565+63_3565+64insACA
NM_001317924.2:c.3085+63_3085+64insACA	NP_001304853.1:n.3085+63_3085+64insACA