Canonical Allele Identifier: CA2670359576
Gene: WDR19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39244281del , CM000666.2:g.39244281del GRCh38
NC_000004.11:g.39245901del , CM000666.1:g.39245901del GRCh37
NC_000004.10:g.38922296del NCBI36
NG_031813.1:g.66878del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399820.8:c.2455del MANE Select ENSP00000382717.3:p.Gln819ArgfsTer4
ENST00000399820.7:c.2455del ENSP00000382717.3:p.Gln819ArgfsTer4
ENST00000506869.5:c.*2036del ENSP00000424319.1:n.*2036del
ENST00000512095.5:n.1453del
NM_025132.3:c.2455del NP_079408.3:p.Gln819ArgfsTer4
XM_011513724.1:c.2467del XP_011512026.1:p.Gln823ArgfsTer4
XM_011513725.1:c.2401del XP_011512027.1:p.Gln801ArgfsTer4
XM_011513726.1:c.1987del XP_011512028.1:p.Gln663ArgfsTer4
XM_011513727.1:c.1987del XP_011512029.1:p.Gln663ArgfsTer4
XM_011513728.1:c.1975del XP_011512030.1:p.Gln659ArgfsTer4
XM_011513729.1:c.2467del XP_011512031.1:p.Gln823ArgfsTer4
XR_925155.1:n.2531del
NM_001317924.1:c.1975del NP_001304853.1:p.Gln659ArgfsTer4
XM_011513725.2:c.2401del XP_011512027.1:p.Gln801ArgfsTer4
XM_011513726.3:c.1987del XP_011512028.1:p.Gln663ArgfsTer4
XM_017008501.1:c.1975del XP_016863990.1:p.Gln659ArgfsTer4
XR_001741306.1:n.2531del
XR_001741307.1:n.2519del
XR_001741308.1:n.2531del
XR_001741309.1:n.2519del
XR_001741310.1:n.2519del
XR_001741311.2:n.2368del
NM_025132.4:c.2455del MANE Select NP_079408.3:p.Gln819ArgfsTer4
NM_001317924.2:c.1975del NP_001304853.1:p.Gln659ArgfsTer4