Canonical Allele Identifier: CA2892186

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39253158T>C , CM000666.2:g.39253158T>C	GRCh38
NC_000004.11:g.39254778T>C , CM000666.1:g.39254778T>C	GRCh37
NC_000004.10:g.38931173T>C	NCBI36
NG_031813.1:g.75755T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2742T>C MANE Select	ENSP00000382717.3:p.Ala914=
ENST00000399820.7:c.2742T>C	ENSP00000382717.3:p.Ala914=
ENST00000506869.5:c.*2323T>C	ENSP00000424319.1:n.*2323T>C
ENST00000512095.5:n.1740T>C
NM_025132.3:c.2742T>C	NP_079408.3:p.Ala914=
XM_011513724.1:c.2754T>C	XP_011512026.1:p.Ala918=
XM_011513725.1:c.2688T>C	XP_011512027.1:p.Ala896=
XM_011513726.1:c.2274T>C	XP_011512028.1:p.Ala758=
XM_011513727.1:c.2274T>C	XP_011512029.1:p.Ala758=
XM_011513728.1:c.2262T>C	XP_011512030.1:p.Ala754=
XM_011513729.1:c.2754T>C	XP_011512031.1:p.Ala918=
XR_925155.1:n.2818T>C
NM_001317924.1:c.2262T>C	NP_001304853.1:p.Ala754=
XM_011513725.2:c.2688T>C	XP_011512027.1:p.Ala896=
XM_011513726.3:c.2274T>C	XP_011512028.1:p.Ala758=
XM_017008501.1:c.2262T>C	XP_016863990.1:p.Ala754=
XR_001741306.1:n.2818T>C
XR_001741307.1:n.2806T>C
XR_001741308.1:n.2818T>C
XR_001741309.1:n.2806T>C
XR_001741310.1:n.2806T>C
XR_001741311.2:n.2655T>C
NM_025132.4:c.2742T>C MANE Select	NP_079408.3:p.Ala914=
NM_001317924.2:c.2262T>C	NP_001304853.1:p.Ala754=