Canonical Allele Identifier: CA438943865

Gene: WDR19

Linked Data

• gnomAD v4: 4-39277023-A-G
• MyVariant Identifiers: chr4:g.39278643A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277023A>G , CM000666.2:g.39277023A>G	GRCh38
NC_000004.11:g.39278643A>G , CM000666.1:g.39278643A>G	GRCh37
NC_000004.10:g.38955038A>G	NCBI36
NG_031813.1:g.99620A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3720A>G MANE Select	ENSP00000382717.3:p.Arg1240=
ENST00000399820.7:c.3720A>G	ENSP00000382717.3:p.Arg1240=
ENST00000503733.1:n.60A>G
ENST00000506869.5:c.*3301A>G	ENSP00000424319.1:n.*3301A>G
ENST00000512534.5:n.2031A>G
ENST00000512588.5:n.62A>G
NM_025132.3:c.3720A>G	NP_079408.3:p.Arg1240=
XM_011513724.1:c.3732A>G	XP_011512026.1:p.Arg1244=
XM_011513725.1:c.3666A>G	XP_011512027.1:p.Arg1222=
XM_011513726.1:c.3252A>G	XP_011512028.1:p.Arg1084=
XM_011513727.1:c.3252A>G	XP_011512029.1:p.Arg1084=
XM_011513728.1:c.3240A>G	XP_011512030.1:p.Arg1080=
XR_925155.1:n.5430A>G
NM_001317924.1:c.3240A>G	NP_001304853.1:p.Arg1080=
XM_011513725.2:c.3666A>G	XP_011512027.1:p.Arg1222=
XM_011513726.3:c.3252A>G	XP_011512028.1:p.Arg1084=
XM_017008501.1:c.3240A>G	XP_016863990.1:p.Arg1080=
XR_001741306.1:n.3997A>G
XR_001741307.1:n.3985A>G
XR_001741308.1:n.5631A>G
XR_001741309.1:n.5418A>G
XR_001741310.1:n.5619A>G
XR_001741311.2:n.5267A>G
NM_025132.4:c.3720A>G MANE Select	NP_079408.3:p.Arg1240=
NM_001317924.2:c.3240A>G	NP_001304853.1:p.Arg1080=