Canonical Allele Identifier: CA356651518

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39278641A>G (hg19) ; chr4:g.39277021A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277021A>G , CM000666.2:g.39277021A>G	GRCh38
NC_000004.11:g.39278641A>G , CM000666.1:g.39278641A>G	GRCh37
NC_000004.10:g.38955036A>G	NCBI36
NG_031813.1:g.99618A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3718A>G MANE Select	ENSP00000382717.3:p.Arg1240Gly
ENST00000399820.7:c.3718A>G	ENSP00000382717.3:p.Arg1240Gly
ENST00000503733.1:n.58A>G
ENST00000506869.5:c.*3299A>G	ENSP00000424319.1:n.*3299A>G
ENST00000512534.5:n.2029A>G
ENST00000512588.5:n.60A>G
NM_025132.3:c.3718A>G	NP_079408.3:p.Arg1240Gly
XM_011513724.1:c.3730A>G	XP_011512026.1:p.Arg1244Gly
XM_011513725.1:c.3664A>G	XP_011512027.1:p.Arg1222Gly
XM_011513726.1:c.3250A>G	XP_011512028.1:p.Arg1084Gly
XM_011513727.1:c.3250A>G	XP_011512029.1:p.Arg1084Gly
XM_011513728.1:c.3238A>G	XP_011512030.1:p.Arg1080Gly
XR_925155.1:n.5428A>G
NM_001317924.1:c.3238A>G	NP_001304853.1:p.Arg1080Gly
XM_011513725.2:c.3664A>G	XP_011512027.1:p.Arg1222Gly
XM_011513726.3:c.3250A>G	XP_011512028.1:p.Arg1084Gly
XM_017008501.1:c.3238A>G	XP_016863990.1:p.Arg1080Gly
XR_001741306.1:n.3995A>G
XR_001741307.1:n.3983A>G
XR_001741308.1:n.5629A>G
XR_001741309.1:n.5416A>G
XR_001741310.1:n.5617A>G
XR_001741311.2:n.5265A>G
NM_025132.4:c.3718A>G MANE Select	NP_079408.3:p.Arg1240Gly
NM_001317924.2:c.3238A>G	NP_001304853.1:p.Arg1080Gly