Canonical Allele Identifier: CA1451994303

Gene: WDR19

Linked Data

• dbSNP Id: rs1727824951

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205264_39205281dup , CM000666.2:g.39205264_39205281dup	GRCh38
NC_000004.11:g.39206884_39206901dup , CM000666.1:g.39206884_39206901dup	GRCh37
NC_000004.10:g.38883279_38883296dup	NCBI36
NG_031813.1:g.27861_27878dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.714_716+15dup
ENST00000399820.7:c.714_716+15dup
ENST00000503697.5:c.*182_*184+15dup
ENST00000505055.5:c.*295_*297+15dup
ENST00000506503.1:c.714_716+15dup
ENST00000506869.5:c.*295_*297+15dup
ENST00000511729.5:n.40+22701_40+22718dup
ENST00000512448.1:n.308_310+15dup
NM_025132.3:c.714_716+15dup
XM_011513724.1:c.714_716+15dup
XM_011513725.1:c.648_650+15dup
XM_011513726.1:c.234_236+15dup
XM_011513727.1:c.234_236+15dup
XM_011513728.1:c.234_236+15dup
XM_011513729.1:c.714_716+15dup
XR_925155.1:n.778_780+15dup
NM_001317924.1:c.234_236+15dup
XM_011513725.2:c.648_650+15dup
XM_011513726.3:c.234_236+15dup
XM_017008501.1:c.234_236+15dup
XR_001741306.1:n.778_780+15dup
XR_001741307.1:n.778_780+15dup
XR_001741308.1:n.778_780+15dup
XR_001741309.1:n.778_780+15dup
XR_001741310.1:n.778_780+15dup
XR_001741311.2:n.627_629+15dup
XR_001741312.1:n.778_780+15dup
NM_025132.4:c.714_716+15dup
NM_001317924.2:c.234_236+15dup