Canonical Allele Identifier: CA2892540

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39278539C>T , CM000666.2:g.39278539C>T	GRCh38
NC_000004.11:g.39280159C>T , CM000666.1:g.39280159C>T	GRCh37
NC_000004.10:g.38956554C>T	NCBI36
NG_031813.1:g.101136C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.3918C>T MANE Select	NP_079408.3:p.Ile1306=
ENST00000399820.8:c.3918C>T MANE Select	ENSP00000382717.3:p.Ile1306=
NM_001317924.1:c.3438C>T	NP_001304853.1:p.Ile1146=
NM_001317924.2:c.3438C>T	NP_001304853.1:p.Ile1146=
NM_025132.3:c.3918C>T	NP_079408.3:p.Ile1306=
ENST00000399820.7:c.3918C>T	ENSP00000382717.3:p.Ile1306=
ENST00000503733.1:n.273C>T
ENST00000506869.5:c.*3499C>T	ENSP00000424319.1:n.*3499C>T
ENST00000510315.1:n.269C>T
ENST00000512534.5:n.2229C>T
ENST00000512588.5:n.260C>T
XM_011513724.1:c.3930C>T	XP_011512026.1:p.Ile1310=
XM_011513725.1:c.3864C>T	XP_011512027.1:p.Ile1288=
XM_011513725.2:c.3864C>T	XP_011512027.1:p.Ile1288=
XM_011513726.1:c.3450C>T	XP_011512028.1:p.Ile1150=
XM_011513726.3:c.3450C>T	XP_011512028.1:p.Ile1150=
XM_011513727.1:c.3450C>T	XP_011512029.1:p.Ile1150=
XM_011513728.1:c.3438C>T	XP_011512030.1:p.Ile1146=
XM_017008501.1:c.3438C>T	XP_016863990.1:p.Ile1146=
XR_001741306.1:n.4195C>T
XR_001741307.1:n.4183C>T
XR_001741308.1:n.5829C>T
XR_001741309.1:n.5616C>T
XR_001741310.1:n.5817C>T
XR_001741311.2:n.5465C>T
XR_925155.1:n.5628C>T