Canonical Allele Identifier: CA356652263

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39278724T>G (hg19) ; chr4:g.39277104T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277104T>G , CM000666.2:g.39277104T>G	GRCh38
NC_000004.11:g.39278724T>G , CM000666.1:g.39278724T>G	GRCh37
NC_000004.10:g.38955119T>G	NCBI36
NG_031813.1:g.99701T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3801T>G MANE Select	ENSP00000382717.3:p.Cys1267Trp
ENST00000399820.7:c.3801T>G	ENSP00000382717.3:p.Cys1267Trp
ENST00000503733.1:n.141T>G
ENST00000506869.5:c.*3382T>G	ENSP00000424319.1:n.*3382T>G
ENST00000512534.5:n.2112T>G
ENST00000512588.5:n.143T>G
NM_025132.3:c.3801T>G	NP_079408.3:p.Cys1267Trp
XM_011513724.1:c.3813T>G	XP_011512026.1:p.Cys1271Trp
XM_011513725.1:c.3747T>G	XP_011512027.1:p.Cys1249Trp
XM_011513726.1:c.3333T>G	XP_011512028.1:p.Cys1111Trp
XM_011513727.1:c.3333T>G	XP_011512029.1:p.Cys1111Trp
XM_011513728.1:c.3321T>G	XP_011512030.1:p.Cys1107Trp
XR_925155.1:n.5511T>G
NM_001317924.1:c.3321T>G	NP_001304853.1:p.Cys1107Trp
XM_011513725.2:c.3747T>G	XP_011512027.1:p.Cys1249Trp
XM_011513726.3:c.3333T>G	XP_011512028.1:p.Cys1111Trp
XM_017008501.1:c.3321T>G	XP_016863990.1:p.Cys1107Trp
XR_001741306.1:n.4078T>G
XR_001741307.1:n.4066T>G
XR_001741308.1:n.5712T>G
XR_001741309.1:n.5499T>G
XR_001741310.1:n.5700T>G
XR_001741311.2:n.5348T>G
NM_025132.4:c.3801T>G MANE Select	NP_079408.3:p.Cys1267Trp
NM_001317924.2:c.3321T>G	NP_001304853.1:p.Cys1107Trp