Canonical Allele Identifier: CA2761116291

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39274951_39274955del , CM000666.2:g.39274951_39274955del	GRCh38
NC_000004.11:g.39276571_39276575del , CM000666.1:g.39276571_39276575del	GRCh37
NC_000004.10:g.38952966_38952970del	NCBI36
NG_031813.1:g.97548_97552del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3709_3713del MANE Select	ENSP00000382717.3:p.Met1237GlnfsTer7
ENST00000399820.7:c.3709_3713del	ENSP00000382717.3:p.Met1237GlnfsTer7
ENST00000506869.5:c.*3290_*3294del	ENSP00000424319.1:n.*3290_*3294del
ENST00000512095.5:n.2707_2711del
ENST00000512534.5:n.2020_2024del
NM_025132.3:c.3709_3713del	NP_079408.3:p.Met1237GlnfsTer7
XM_011513724.1:c.3721_3725del	XP_011512026.1:p.Met1241GlnfsTer7
XM_011513725.1:c.3655_3659del	XP_011512027.1:p.Met1219GlnfsTer7
XM_011513726.1:c.3241_3245del	XP_011512028.1:p.Met1081GlnfsTer7
XM_011513727.1:c.3241_3245del	XP_011512029.1:p.Met1081GlnfsTer7
XM_011513728.1:c.3229_3233del	XP_011512030.1:p.Met1077GlnfsTer7
XR_925155.1:n.5419_5423del
NM_001317924.1:c.3229_3233del	NP_001304853.1:p.Met1077GlnfsTer7
XM_011513725.2:c.3655_3659del	XP_011512027.1:p.Met1219GlnfsTer7
XM_011513726.3:c.3241_3245del	XP_011512028.1:p.Met1081GlnfsTer7
XM_017008501.1:c.3229_3233del	XP_016863990.1:p.Met1077GlnfsTer7
XR_001741306.1:n.3785_3789del
XR_001741307.1:n.3773_3777del
XR_001741308.1:n.5419_5423del
XR_001741309.1:n.5407_5411del
XR_001741310.1:n.5407_5411del
XR_001741311.2:n.5256_5260del
NM_025132.4:c.3709_3713del MANE Select	NP_079408.3:p.Met1237GlnfsTer7
NM_001317924.2:c.3229_3233del	NP_001304853.1:p.Met1077GlnfsTer7