Canonical Allele Identifier: CA356647613

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39274679C>G (hg19) ; chr4:g.39273059C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273059C>G , CM000666.2:g.39273059C>G	GRCh38
NC_000004.11:g.39274679C>G , CM000666.1:g.39274679C>G	GRCh37
NC_000004.10:g.38951074C>G	NCBI36
NG_031813.1:g.95656C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3563C>G MANE Select	ENSP00000382717.3:p.Ser1188Ter
ENST00000399820.7:c.3563C>G	ENSP00000382717.3:p.Ser1188Ter
ENST00000506869.5:c.*3144C>G	ENSP00000424319.1:n.*3144C>G
ENST00000512095.5:n.2561C>G
ENST00000512534.5:n.128C>G
NM_025132.3:c.3563C>G	NP_079408.3:p.Ser1188Ter
XM_011513724.1:c.3575C>G	XP_011512026.1:p.Ser1192Ter
XM_011513725.1:c.3509C>G	XP_011512027.1:p.Ser1170Ter
XM_011513726.1:c.3095C>G	XP_011512028.1:p.Ser1032Ter
XM_011513727.1:c.3095C>G	XP_011512029.1:p.Ser1032Ter
XM_011513728.1:c.3083C>G	XP_011512030.1:p.Ser1028Ter
XR_925155.1:n.3639C>G
NM_001317924.1:c.3083C>G	NP_001304853.1:p.Ser1028Ter
XM_011513725.2:c.3509C>G	XP_011512027.1:p.Ser1170Ter
XM_011513726.3:c.3095C>G	XP_011512028.1:p.Ser1032Ter
XM_017008501.1:c.3083C>G	XP_016863990.1:p.Ser1028Ter
XR_001741306.1:n.3639C>G
XR_001741307.1:n.3627C>G
XR_001741308.1:n.3639C>G
XR_001741309.1:n.3627C>G
XR_001741310.1:n.3627C>G
XR_001741311.2:n.3476C>G
NM_025132.4:c.3563C>G MANE Select	NP_079408.3:p.Ser1188Ter
NM_001317924.2:c.3083C>G	NP_001304853.1:p.Ser1028Ter