Canonical Allele Identifier: CA2761114618

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244445_39244446insAG , CM000666.2:g.39244445_39244446insAG	GRCh38
NC_000004.11:g.39246065_39246066insAG , CM000666.1:g.39246065_39246066insAG	GRCh37
NC_000004.10:g.38922460_38922461insAG	NCBI36
NG_031813.1:g.67042_67043insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2563-25_2563-24insAG MANE Select	ENSP00000382717.3:n.2563-25_2563-24insAG
ENST00000399820.7:c.2563-25_2563-24insAG	ENSP00000382717.3:n.2563-25_2563-24insAG
ENST00000506869.5:c.*2144-25_*2144-24insAG	ENSP00000424319.1:n.*2144-25_*2144-24insAG
ENST00000512095.5:n.1561-25_1561-24insAG
NM_025132.3:c.2563-25_2563-24insAG	NP_079408.3:n.2563-25_2563-24insAG
XM_011513724.1:c.2575-25_2575-24insAG	XP_011512026.1:n.2575-25_2575-24insAG
XM_011513725.1:c.2509-25_2509-24insAG	XP_011512027.1:n.2509-25_2509-24insAG
XM_011513726.1:c.2095-25_2095-24insAG	XP_011512028.1:n.2095-25_2095-24insAG
XM_011513727.1:c.2095-25_2095-24insAG	XP_011512029.1:n.2095-25_2095-24insAG
XM_011513728.1:c.2083-25_2083-24insAG	XP_011512030.1:n.2083-25_2083-24insAG
XM_011513729.1:c.2575-25_2575-24insAG	XP_011512031.1:n.2575-25_2575-24insAG
XR_925155.1:n.2639-25_2639-24insAG
NM_001317924.1:c.2083-25_2083-24insAG	NP_001304853.1:n.2083-25_2083-24insAG
XM_011513725.2:c.2509-25_2509-24insAG	XP_011512027.1:n.2509-25_2509-24insAG
XM_011513726.3:c.2095-25_2095-24insAG	XP_011512028.1:n.2095-25_2095-24insAG
XM_017008501.1:c.2083-25_2083-24insAG	XP_016863990.1:n.2083-25_2083-24insAG
XR_001741306.1:n.2639-25_2639-24insAG
XR_001741307.1:n.2627-25_2627-24insAG
XR_001741308.1:n.2639-25_2639-24insAG
XR_001741309.1:n.2627-25_2627-24insAG
XR_001741310.1:n.2627-25_2627-24insAG
XR_001741311.2:n.2476-25_2476-24insAG
NM_025132.4:c.2563-25_2563-24insAG MANE Select	NP_079408.3:n.2563-25_2563-24insAG
NM_001317924.2:c.2083-25_2083-24insAG	NP_001304853.1:n.2083-25_2083-24insAG