Canonical Allele Identifier: CA356641737

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39253916C>T , CM000666.2:g.39253916C>T	GRCh38
NC_000004.11:g.39255536C>T , CM000666.1:g.39255536C>T	GRCh37
NC_000004.10:g.38931931C>T	NCBI36
NG_031813.1:g.76513C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.2887C>T MANE Select	NP_079408.3:p.Gln963Ter
ENST00000399820.8:c.2887C>T MANE Select	ENSP00000382717.3:p.Gln963Ter
NM_001317924.1:c.2407C>T	NP_001304853.1:p.Gln803Ter
NM_001317924.2:c.2407C>T	NP_001304853.1:p.Gln803Ter
NM_025132.3:c.2887C>T	NP_079408.3:p.Gln963Ter
ENST00000399820.7:c.2887C>T	ENSP00000382717.3:p.Gln963Ter
ENST00000506869.5:c.*2468C>T	ENSP00000424319.1:n.*2468C>T
ENST00000512095.5:n.1885C>T
XM_011513724.1:c.2899C>T	XP_011512026.1:p.Gln967Ter
XM_011513725.1:c.2833C>T	XP_011512027.1:p.Gln945Ter
XM_011513725.2:c.2833C>T	XP_011512027.1:p.Gln945Ter
XM_011513726.1:c.2419C>T	XP_011512028.1:p.Gln807Ter
XM_011513726.3:c.2419C>T	XP_011512028.1:p.Gln807Ter
XM_011513727.1:c.2419C>T	XP_011512029.1:p.Gln807Ter
XM_011513728.1:c.2407C>T	XP_011512030.1:p.Gln803Ter
XM_011513729.1:c.2900C>T	XP_011512031.1:p.Thr967Ile
XM_017008501.1:c.2407C>T	XP_016863990.1:p.Gln803Ter
XR_001741306.1:n.2963C>T
XR_001741307.1:n.2951C>T
XR_001741308.1:n.2963C>T
XR_001741309.1:n.2951C>T
XR_001741310.1:n.2951C>T
XR_001741311.2:n.2800C>T
XR_925155.1:n.2963C>T