Canonical Allele Identifier: CA356652276

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39278726C>A (hg19) ; chr4:g.39277106C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277106C>A , CM000666.2:g.39277106C>A	GRCh38
NC_000004.11:g.39278726C>A , CM000666.1:g.39278726C>A	GRCh37
NC_000004.10:g.38955121C>A	NCBI36
NG_031813.1:g.99703C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3803C>A MANE Select	ENSP00000382717.3:p.Pro1268His
ENST00000399820.7:c.3803C>A	ENSP00000382717.3:p.Pro1268His
ENST00000503733.1:n.143C>A
ENST00000506869.5:c.*3384C>A	ENSP00000424319.1:n.*3384C>A
ENST00000512534.5:n.2114C>A
ENST00000512588.5:n.145C>A
NM_025132.3:c.3803C>A	NP_079408.3:p.Pro1268His
XM_011513724.1:c.3815C>A	XP_011512026.1:p.Pro1272His
XM_011513725.1:c.3749C>A	XP_011512027.1:p.Pro1250His
XM_011513726.1:c.3335C>A	XP_011512028.1:p.Pro1112His
XM_011513727.1:c.3335C>A	XP_011512029.1:p.Pro1112His
XM_011513728.1:c.3323C>A	XP_011512030.1:p.Pro1108His
XR_925155.1:n.5513C>A
NM_001317924.1:c.3323C>A	NP_001304853.1:p.Pro1108His
XM_011513725.2:c.3749C>A	XP_011512027.1:p.Pro1250His
XM_011513726.3:c.3335C>A	XP_011512028.1:p.Pro1112His
XM_017008501.1:c.3323C>A	XP_016863990.1:p.Pro1108His
XR_001741306.1:n.4080C>A
XR_001741307.1:n.4068C>A
XR_001741308.1:n.5714C>A
XR_001741309.1:n.5501C>A
XR_001741310.1:n.5702C>A
XR_001741311.2:n.5350C>A
NM_025132.4:c.3803C>A MANE Select	NP_079408.3:p.Pro1268His
NM_001317924.2:c.3323C>A	NP_001304853.1:p.Pro1108His