Canonical Allele Identifier: CA356634370
Gene: WDR19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39205636C>A , CM000666.2:g.39205636C>A GRCh38
NC_000004.11:g.39207256C>A , CM000666.1:g.39207256C>A GRCh37
NC_000004.10:g.38883651C>A NCBI36
NG_031813.1:g.28233C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.790C>A MANE Select ENSP00000382717.3:p.Leu264Ile
ENST00000399820.7:c.790C>A ENSP00000382717.3:p.Leu264Ile
ENST00000503697.5:c.*258C>A ENSP00000423706.1:n.*258C>A
ENST00000506503.1:c.790C>A ENSP00000423491.1:p.Leu264Ile
ENST00000506869.5:c.*371C>A ENSP00000424319.1:n.*371C>A
ENST00000511729.5:n.41-22922C>A
ENST00000512448.1:n.384C>A
NM_025132.3:c.790C>A NP_079408.3:p.Leu264Ile
XM_011513724.1:c.790C>A XP_011512026.1:p.Leu264Ile
XM_011513725.1:c.724C>A XP_011512027.1:p.Leu242Ile
XM_011513726.1:c.310C>A XP_011512028.1:p.Leu104Ile
XM_011513727.1:c.310C>A XP_011512029.1:p.Leu104Ile
XM_011513728.1:c.310C>A XP_011512030.1:p.Leu104Ile
XM_011513729.1:c.790C>A XP_011512031.1:p.Leu264Ile
XR_925155.1:n.854C>A
NM_001317924.1:c.310C>A NP_001304853.1:p.Leu104Ile
XM_011513725.2:c.724C>A XP_011512027.1:p.Leu242Ile
XM_011513726.3:c.310C>A XP_011512028.1:p.Leu104Ile
XM_017008501.1:c.310C>A XP_016863990.1:p.Leu104Ile
XR_001741306.1:n.854C>A
XR_001741307.1:n.854C>A
XR_001741308.1:n.854C>A
XR_001741309.1:n.854C>A
XR_001741310.1:n.854C>A
XR_001741311.2:n.703C>A
XR_001741312.1:n.854C>A
NM_025132.4:c.790C>A MANE Select NP_079408.3:p.Leu264Ile
NM_001317924.2:c.310C>A NP_001304853.1:p.Leu104Ile