Canonical Allele Identifier: CA1452052331

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39231943T= , CM000666.2:g.39231943T=	GRCh38
NC_000004.11:g.39233563T= , CM000666.1:g.39233563T=	GRCh37
NC_000004.10:g.38909958T=	NCBI36
NG_031813.1:g.54540T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2129T= MANE Select	ENSP00000382717.3:p.Leu710=
ENST00000399820.7:c.2129T=	ENSP00000382717.3:p.Leu710=
ENST00000506869.5:c.*1710T=	ENSP00000424319.1:n.*1710T=
ENST00000507228.1:c.307T=
ENST00000511729.5:n.320T=
ENST00000512095.5:n.1127T=
ENST00000515631.1:n.283T=
NM_025132.3:c.2129T=	NP_079408.3:p.Leu710=
XM_011513724.1:c.2129T=	XP_011512026.1:p.Leu710=
XM_011513725.1:c.2063T=	XP_011512027.1:p.Leu688=
XM_011513726.1:c.1649T=	XP_011512028.1:p.Leu550=
XM_011513727.1:c.1649T=	XP_011512029.1:p.Leu550=
XM_011513728.1:c.1649T=	XP_011512030.1:p.Leu550=
XM_011513729.1:c.2129T=	XP_011512031.1:p.Leu710=
XR_925155.1:n.2193T=
NM_001317924.1:c.1649T=	NP_001304853.1:p.Leu550=
XM_011513725.2:c.2063T=	XP_011512027.1:p.Leu688=
XM_011513726.3:c.1649T=	XP_011512028.1:p.Leu550=
XM_017008501.1:c.1649T=	XP_016863990.1:p.Leu550=
XR_001741306.1:n.2193T=
XR_001741307.1:n.2193T=
XR_001741308.1:n.2193T=
XR_001741309.1:n.2193T=
XR_001741310.1:n.2193T=
XR_001741311.2:n.2042T=
XR_001741312.1:n.2193T=
NM_025132.4:c.2129T= MANE Select	NP_079408.3:p.Leu710=
NM_001317924.2:c.1649T=	NP_001304853.1:p.Leu550=