Canonical Allele Identifier: CA438943439

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39274635T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273015T>G , CM000666.2:g.39273015T>G	GRCh38
NC_000004.11:g.39274635T>G , CM000666.1:g.39274635T>G	GRCh37
NC_000004.10:g.38951030T>G	NCBI36
NG_031813.1:g.95612T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3519T>G MANE Select	ENSP00000382717.3:p.Ala1173=
ENST00000399820.7:c.3519T>G	ENSP00000382717.3:p.Ala1173=
ENST00000506869.5:c.*3100T>G	ENSP00000424319.1:n.*3100T>G
ENST00000512095.5:n.2517T>G
ENST00000512534.5:n.84T>G
NM_025132.3:c.3519T>G	NP_079408.3:p.Ala1173=
XM_011513724.1:c.3531T>G	XP_011512026.1:p.Ala1177=
XM_011513725.1:c.3465T>G	XP_011512027.1:p.Ala1155=
XM_011513726.1:c.3051T>G	XP_011512028.1:p.Ala1017=
XM_011513727.1:c.3051T>G	XP_011512029.1:p.Ala1017=
XM_011513728.1:c.3039T>G	XP_011512030.1:p.Ala1013=
XR_925155.1:n.3595T>G
NM_001317924.1:c.3039T>G	NP_001304853.1:p.Ala1013=
XM_011513725.2:c.3465T>G	XP_011512027.1:p.Ala1155=
XM_011513726.3:c.3051T>G	XP_011512028.1:p.Ala1017=
XM_017008501.1:c.3039T>G	XP_016863990.1:p.Ala1013=
XR_001741306.1:n.3595T>G
XR_001741307.1:n.3583T>G
XR_001741308.1:n.3595T>G
XR_001741309.1:n.3583T>G
XR_001741310.1:n.3583T>G
XR_001741311.2:n.3432T>G
NM_025132.4:c.3519T>G MANE Select	NP_079408.3:p.Ala1173=
NM_001317924.2:c.3039T>G	NP_001304853.1:p.Ala1013=