Canonical Allele Identifier: CA356631600

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39189766T>A , CM000666.2:g.39189766T>A	GRCh38
NC_000004.11:g.39191386T>A , CM000666.1:g.39191386T>A	GRCh37
NC_000004.10:g.38867781T>A	NCBI36
NG_031813.1:g.12363T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.275T>A MANE Select	NP_079408.3:p.Leu92Ter
ENST00000399820.8:c.275T>A MANE Select	ENSP00000382717.3:p.Leu92Ter
NM_001317924.1:c.-90T>A	NP_001304853.1:n.-90T>A
NM_001317924.2:c.-90T>A	NP_001304853.1:n.-90T>A
NM_025132.3:c.275T>A	NP_079408.3:p.Leu92Ter
ENST00000399820.7:c.275T>A	ENSP00000382717.3:p.Leu92Ter
ENST00000502389.1:n.302T>A
ENST00000503697.5:c.275T>A	ENSP00000423706.1:p.Leu92Ter
ENST00000505055.5:c.209T>A	ENSP00000425949.1:p.Leu70Ter
ENST00000506503.1:c.275T>A	ENSP00000423491.1:p.Leu92Ter
ENST00000506869.5:c.275T>A	ENSP00000424319.1:p.Leu92Ter
ENST00000509560.5:c.98T>A	ENSP00000426918.1:p.Leu33Ter
ENST00000511729.5:n.40+7203T>A
ENST00000512112.5:c.-90T>A	ENSP00000421888.1:n.-90T>A
XM_011513724.1:c.275T>A	XP_011512026.1:p.Leu92Ter
XM_011513725.1:c.209T>A	XP_011512027.1:p.Leu70Ter
XM_011513725.2:c.209T>A	XP_011512027.1:p.Leu70Ter
XM_011513726.1:c.-90T>A	XP_011512028.1:n.-90T>A
XM_011513726.3:c.-90T>A	XP_011512028.1:n.-90T>A
XM_011513727.1:c.-90T>A	XP_011512029.1:n.-90T>A
XM_011513728.1:c.-90T>A	XP_011512030.1:n.-90T>A
XM_011513729.1:c.275T>A	XP_011512031.1:p.Leu92Ter
XM_017008501.1:c.-90T>A	XP_016863990.1:n.-90T>A
XR_001741306.1:n.339T>A
XR_001741307.1:n.339T>A
XR_001741308.1:n.339T>A
XR_001741309.1:n.339T>A
XR_001741310.1:n.339T>A
XR_001741311.2:n.304T>A
XR_001741312.1:n.339T>A
XR_925155.1:n.339T>A