Canonical Allele Identifier: CA356651556

Gene: WDR19

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3722C>G MANE Select	ENSP00000382717.3:p.Pro1241Arg
ENST00000399820.7:c.3722C>G	ENSP00000382717.3:p.Pro1241Arg
ENST00000503733.1:n.62C>G
ENST00000506869.5:c.*3303C>G	ENSP00000424319.1:n.*3303C>G
ENST00000512534.5:n.2033C>G
ENST00000512588.5:n.64C>G
NM_025132.3:c.3722C>G	NP_079408.3:p.Pro1241Arg
XM_011513724.1:c.3734C>G	XP_011512026.1:p.Pro1245Arg
XM_011513725.1:c.3668C>G	XP_011512027.1:p.Pro1223Arg
XM_011513726.1:c.3254C>G	XP_011512028.1:p.Pro1085Arg
XM_011513727.1:c.3254C>G	XP_011512029.1:p.Pro1085Arg
XM_011513728.1:c.3242C>G	XP_011512030.1:p.Pro1081Arg
XR_925155.1:n.5432C>G
NM_001317924.1:c.3242C>G	NP_001304853.1:p.Pro1081Arg
XM_011513725.2:c.3668C>G	XP_011512027.1:p.Pro1223Arg
XM_011513726.3:c.3254C>G	XP_011512028.1:p.Pro1085Arg
XM_017008501.1:c.3242C>G	XP_016863990.1:p.Pro1081Arg
XR_001741306.1:n.3999C>G
XR_001741307.1:n.3987C>G
XR_001741308.1:n.5633C>G
XR_001741309.1:n.5420C>G
XR_001741310.1:n.5621C>G
XR_001741311.2:n.5269C>G
NM_025132.4:c.3722C>G MANE Select	NP_079408.3:p.Pro1241Arg
NM_001317924.2:c.3242C>G	NP_001304853.1:p.Pro1081Arg