Canonical Allele Identifier: CA2761114640

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244604_39244605insACAA , CM000666.2:g.39244604_39244605insACAA	GRCh38
NC_000004.11:g.39246224_39246225insACAA , CM000666.1:g.39246224_39246225insACAA	GRCh37
NC_000004.10:g.38922619_38922620insACAA	NCBI36
NG_031813.1:g.67201_67202insACAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2645+52_2645+53insACAA MANE Select	ENSP00000382717.3:n.2645+52_2645+53insACAA
ENST00000399820.7:c.2645+52_2645+53insACAA	ENSP00000382717.3:n.2645+52_2645+53insACAA
ENST00000506869.5:c.*2226+52_*2226+53insACAA	ENSP00000424319.1:n.*2226+52_*2226+53insACAA
ENST00000512095.5:n.1643+52_1643+53insACAA
NM_025132.3:c.2645+52_2645+53insACAA	NP_079408.3:n.2645+52_2645+53insACAA
XM_011513724.1:c.2657+52_2657+53insACAA	XP_011512026.1:n.2657+52_2657+53insACAA
XM_011513725.1:c.2591+52_2591+53insACAA	XP_011512027.1:n.2591+52_2591+53insACAA
XM_011513726.1:c.2177+52_2177+53insACAA	XP_011512028.1:n.2177+52_2177+53insACAA
XM_011513727.1:c.2177+52_2177+53insACAA	XP_011512029.1:n.2177+52_2177+53insACAA
XM_011513728.1:c.2165+52_2165+53insACAA	XP_011512030.1:n.2165+52_2165+53insACAA
XM_011513729.1:c.2657+52_2657+53insACAA	XP_011512031.1:n.2657+52_2657+53insACAA
XR_925155.1:n.2721+52_2721+53insACAA
NM_001317924.1:c.2165+52_2165+53insACAA	NP_001304853.1:n.2165+52_2165+53insACAA
XM_011513725.2:c.2591+52_2591+53insACAA	XP_011512027.1:n.2591+52_2591+53insACAA
XM_011513726.3:c.2177+52_2177+53insACAA	XP_011512028.1:n.2177+52_2177+53insACAA
XM_017008501.1:c.2165+52_2165+53insACAA	XP_016863990.1:n.2165+52_2165+53insACAA
XR_001741306.1:n.2721+52_2721+53insACAA
XR_001741307.1:n.2709+52_2709+53insACAA
XR_001741308.1:n.2721+52_2721+53insACAA
XR_001741309.1:n.2709+52_2709+53insACAA
XR_001741310.1:n.2709+52_2709+53insACAA
XR_001741311.2:n.2558+52_2558+53insACAA
NM_025132.4:c.2645+52_2645+53insACAA MANE Select	NP_079408.3:n.2645+52_2645+53insACAA
NM_001317924.2:c.2165+52_2165+53insACAA	NP_001304853.1:n.2165+52_2165+53insACAA