Canonical Allele Identifier: CA2761112797

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205447_39205448insA , CM000666.2:g.39205447_39205448insA	GRCh38
NC_000004.11:g.39207067_39207068insA , CM000666.1:g.39207067_39207068insA	GRCh37
NC_000004.10:g.38883462_38883463insA	NCBI36
NG_031813.1:g.28044_28045insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.717-116_717-115insA MANE Select	ENSP00000382717.3:n.717-116_717-115insA
ENST00000399820.7:c.717-116_717-115insA	ENSP00000382717.3:n.717-116_717-115insA
ENST00000503697.5:c.*185-116_*185-115insA	ENSP00000423706.1:n.*185-116_*185-115insA
ENST00000505055.5:c.*298-116_*298-115insA	ENSP00000425949.1:n.*298-116_*298-115insA
ENST00000506503.1:c.717-116_717-115insA	ENSP00000423491.1:n.717-116_717-115insA
ENST00000506869.5:c.*298-116_*298-115insA	ENSP00000424319.1:n.*298-116_*298-115insA
ENST00000511729.5:n.40+22884_40+22885insA
ENST00000512448.1:n.311-116_311-115insA
NM_025132.3:c.717-116_717-115insA	NP_079408.3:n.717-116_717-115insA
XM_011513724.1:c.717-116_717-115insA	XP_011512026.1:n.717-116_717-115insA
XM_011513725.1:c.651-116_651-115insA	XP_011512027.1:n.651-116_651-115insA
XM_011513726.1:c.237-116_237-115insA	XP_011512028.1:n.237-116_237-115insA
XM_011513727.1:c.237-116_237-115insA	XP_011512029.1:n.237-116_237-115insA
XM_011513728.1:c.237-116_237-115insA	XP_011512030.1:n.237-116_237-115insA
XM_011513729.1:c.717-116_717-115insA	XP_011512031.1:n.717-116_717-115insA
XR_925155.1:n.781-116_781-115insA
NM_001317924.1:c.237-116_237-115insA	NP_001304853.1:n.237-116_237-115insA
XM_011513725.2:c.651-116_651-115insA	XP_011512027.1:n.651-116_651-115insA
XM_011513726.3:c.237-116_237-115insA	XP_011512028.1:n.237-116_237-115insA
XM_017008501.1:c.237-116_237-115insA	XP_016863990.1:n.237-116_237-115insA
XR_001741306.1:n.781-116_781-115insA
XR_001741307.1:n.781-116_781-115insA
XR_001741308.1:n.781-116_781-115insA
XR_001741309.1:n.781-116_781-115insA
XR_001741310.1:n.781-116_781-115insA
XR_001741311.2:n.630-116_630-115insA
XR_001741312.1:n.781-116_781-115insA
NM_025132.4:c.717-116_717-115insA MANE Select	NP_079408.3:n.717-116_717-115insA
NM_001317924.2:c.237-116_237-115insA	NP_001304853.1:n.237-116_237-115insA