Canonical Allele Identifier: CA356652328

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39278733T>G (hg19) ; chr4:g.39277113T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277113T>G , CM000666.2:g.39277113T>G	GRCh38
NC_000004.11:g.39278733T>G , CM000666.1:g.39278733T>G	GRCh37
NC_000004.10:g.38955128T>G	NCBI36
NG_031813.1:g.99710T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3810T>G MANE Select	ENSP00000382717.3:p.Cys1270Trp
ENST00000399820.7:c.3810T>G	ENSP00000382717.3:p.Cys1270Trp
ENST00000503733.1:n.150T>G
ENST00000506869.5:c.*3391T>G	ENSP00000424319.1:n.*3391T>G
ENST00000512534.5:n.2121T>G
ENST00000512588.5:n.152T>G
NM_025132.3:c.3810T>G	NP_079408.3:p.Cys1270Trp
XM_011513724.1:c.3822T>G	XP_011512026.1:p.Cys1274Trp
XM_011513725.1:c.3756T>G	XP_011512027.1:p.Cys1252Trp
XM_011513726.1:c.3342T>G	XP_011512028.1:p.Cys1114Trp
XM_011513727.1:c.3342T>G	XP_011512029.1:p.Cys1114Trp
XM_011513728.1:c.3330T>G	XP_011512030.1:p.Cys1110Trp
XR_925155.1:n.5520T>G
NM_001317924.1:c.3330T>G	NP_001304853.1:p.Cys1110Trp
XM_011513725.2:c.3756T>G	XP_011512027.1:p.Cys1252Trp
XM_011513726.3:c.3342T>G	XP_011512028.1:p.Cys1114Trp
XM_017008501.1:c.3330T>G	XP_016863990.1:p.Cys1110Trp
XR_001741306.1:n.4087T>G
XR_001741307.1:n.4075T>G
XR_001741308.1:n.5721T>G
XR_001741309.1:n.5508T>G
XR_001741310.1:n.5709T>G
XR_001741311.2:n.5357T>G
NM_025132.4:c.3810T>G MANE Select	NP_079408.3:p.Cys1270Trp
NM_001317924.2:c.3330T>G	NP_001304853.1:p.Cys1110Trp