Canonical Allele Identifier: CA2761114644

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244608_39244609insACA , CM000666.2:g.39244608_39244609insACA	GRCh38
NC_000004.11:g.39246228_39246229insACA , CM000666.1:g.39246228_39246229insACA	GRCh37
NC_000004.10:g.38922623_38922624insACA	NCBI36
NG_031813.1:g.67205_67206insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2645+56_2645+57insACA MANE Select	ENSP00000382717.3:n.2645+56_2645+57insACA
ENST00000399820.7:c.2645+56_2645+57insACA	ENSP00000382717.3:n.2645+56_2645+57insACA
ENST00000506869.5:c.*2226+56_*2226+57insACA	ENSP00000424319.1:n.*2226+56_*2226+57insACA
ENST00000512095.5:n.1643+56_1643+57insACA
NM_025132.3:c.2645+56_2645+57insACA	NP_079408.3:n.2645+56_2645+57insACA
XM_011513724.1:c.2657+56_2657+57insACA	XP_011512026.1:n.2657+56_2657+57insACA
XM_011513725.1:c.2591+56_2591+57insACA	XP_011512027.1:n.2591+56_2591+57insACA
XM_011513726.1:c.2177+56_2177+57insACA	XP_011512028.1:n.2177+56_2177+57insACA
XM_011513727.1:c.2177+56_2177+57insACA	XP_011512029.1:n.2177+56_2177+57insACA
XM_011513728.1:c.2165+56_2165+57insACA	XP_011512030.1:n.2165+56_2165+57insACA
XM_011513729.1:c.2657+56_2657+57insACA	XP_011512031.1:n.2657+56_2657+57insACA
XR_925155.1:n.2721+56_2721+57insACA
NM_001317924.1:c.2165+56_2165+57insACA	NP_001304853.1:n.2165+56_2165+57insACA
XM_011513725.2:c.2591+56_2591+57insACA	XP_011512027.1:n.2591+56_2591+57insACA
XM_011513726.3:c.2177+56_2177+57insACA	XP_011512028.1:n.2177+56_2177+57insACA
XM_017008501.1:c.2165+56_2165+57insACA	XP_016863990.1:n.2165+56_2165+57insACA
XR_001741306.1:n.2721+56_2721+57insACA
XR_001741307.1:n.2709+56_2709+57insACA
XR_001741308.1:n.2721+56_2721+57insACA
XR_001741309.1:n.2709+56_2709+57insACA
XR_001741310.1:n.2709+56_2709+57insACA
XR_001741311.2:n.2558+56_2558+57insACA
NM_025132.4:c.2645+56_2645+57insACA MANE Select	NP_079408.3:n.2645+56_2645+57insACA
NM_001317924.2:c.2165+56_2165+57insACA	NP_001304853.1:n.2165+56_2165+57insACA