Canonical Allele Identifier: CA2761112830

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205735_39205749del , CM000666.2:g.39205735_39205749del	GRCh38
NC_000004.11:g.39207355_39207369del , CM000666.1:g.39207355_39207369del	GRCh37
NC_000004.10:g.38883750_38883764del	NCBI36
NG_031813.1:g.28332_28346del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.889_890+13del
ENST00000399820.7:c.889_890+13del
ENST00000503697.5:c.*357_*358+13del
ENST00000506503.1:c.889_890+13del
ENST00000506869.5:c.*470_*471+13del
ENST00000511729.5:n.41-22823_41-22809del
ENST00000512448.1:n.483_497del
NM_025132.3:c.889_890+13del
XM_011513724.1:c.889_890+13del
XM_011513725.1:c.823_824+13del
XM_011513726.1:c.409_410+13del
XM_011513727.1:c.409_410+13del
XM_011513728.1:c.409_410+13del
XM_011513729.1:c.889_890+13del
XR_925155.1:n.953_954+13del
NM_001317924.1:c.409_410+13del
XM_011513725.2:c.823_824+13del
XM_011513726.3:c.409_410+13del
XM_017008501.1:c.409_410+13del
XR_001741306.1:n.953_954+13del
XR_001741307.1:n.953_954+13del
XR_001741308.1:n.953_954+13del
XR_001741309.1:n.953_954+13del
XR_001741310.1:n.953_954+13del
XR_001741311.2:n.802_803+13del
XR_001741312.1:n.953_954+13del
NM_025132.4:c.889_890+13del
NM_001317924.2:c.409_410+13del