Canonical Allele Identifier: CA356651553

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39278645C>A (hg19) ; chr4:g.39277025C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277025C>A , CM000666.2:g.39277025C>A	GRCh38
NC_000004.11:g.39278645C>A , CM000666.1:g.39278645C>A	GRCh37
NC_000004.10:g.38955040C>A	NCBI36
NG_031813.1:g.99622C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3722C>A MANE Select	ENSP00000382717.3:p.Pro1241His
ENST00000399820.7:c.3722C>A	ENSP00000382717.3:p.Pro1241His
ENST00000503733.1:n.62C>A
ENST00000506869.5:c.*3303C>A	ENSP00000424319.1:n.*3303C>A
ENST00000512534.5:n.2033C>A
ENST00000512588.5:n.64C>A
NM_025132.3:c.3722C>A	NP_079408.3:p.Pro1241His
XM_011513724.1:c.3734C>A	XP_011512026.1:p.Pro1245His
XM_011513725.1:c.3668C>A	XP_011512027.1:p.Pro1223His
XM_011513726.1:c.3254C>A	XP_011512028.1:p.Pro1085His
XM_011513727.1:c.3254C>A	XP_011512029.1:p.Pro1085His
XM_011513728.1:c.3242C>A	XP_011512030.1:p.Pro1081His
XR_925155.1:n.5432C>A
NM_001317924.1:c.3242C>A	NP_001304853.1:p.Pro1081His
XM_011513725.2:c.3668C>A	XP_011512027.1:p.Pro1223His
XM_011513726.3:c.3254C>A	XP_011512028.1:p.Pro1085His
XM_017008501.1:c.3242C>A	XP_016863990.1:p.Pro1081His
XR_001741306.1:n.3999C>A
XR_001741307.1:n.3987C>A
XR_001741308.1:n.5633C>A
XR_001741309.1:n.5420C>A
XR_001741310.1:n.5621C>A
XR_001741311.2:n.5269C>A
NM_025132.4:c.3722C>A MANE Select	NP_079408.3:p.Pro1241His
NM_001317924.2:c.3242C>A	NP_001304853.1:p.Pro1081His