Canonical Allele Identifier: CA2892556

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39278635G>A , CM000666.2:g.39278635G>A	GRCh38
NC_000004.11:g.39280255G>A , CM000666.1:g.39280255G>A	GRCh37
NC_000004.10:g.38956650G>A	NCBI36
NG_031813.1:g.101232G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.4014G>A MANE Select	NP_079408.3:p.Thr1338=
ENST00000399820.8:c.4014G>A MANE Select	ENSP00000382717.3:p.Thr1338=
NM_001317924.1:c.3534G>A	NP_001304853.1:p.Thr1178=
NM_001317924.2:c.3534G>A	NP_001304853.1:p.Thr1178=
NM_025132.3:c.4014G>A	NP_079408.3:p.Thr1338=
ENST00000399820.7:c.4014G>A	ENSP00000382717.3:p.Thr1338=
ENST00000503733.1:n.369G>A
ENST00000506869.5:c.*3595G>A	ENSP00000424319.1:n.*3595G>A
ENST00000510315.1:n.365G>A
ENST00000512534.5:n.2325G>A
ENST00000512588.5:n.356G>A
XM_011513724.1:c.4026G>A	XP_011512026.1:p.Thr1342=
XM_011513725.1:c.3960G>A	XP_011512027.1:p.Thr1320=
XM_011513725.2:c.3960G>A	XP_011512027.1:p.Thr1320=
XM_011513726.1:c.3546G>A	XP_011512028.1:p.Thr1182=
XM_011513726.3:c.3546G>A	XP_011512028.1:p.Thr1182=
XM_011513727.1:c.3546G>A	XP_011512029.1:p.Thr1182=
XM_011513728.1:c.3534G>A	XP_011512030.1:p.Thr1178=
XM_017008501.1:c.3534G>A	XP_016863990.1:p.Thr1178=
XR_001741306.1:n.4291G>A
XR_001741307.1:n.4279G>A
XR_001741308.1:n.5925G>A
XR_001741309.1:n.5712G>A
XR_001741310.1:n.5913G>A
XR_001741311.2:n.5561G>A
XR_925155.1:n.5724G>A