Canonical Allele Identifier: CA356634429

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39207283A>T (hg19) ; chr4:g.39205663A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205663A>T , CM000666.2:g.39205663A>T	GRCh38
NC_000004.11:g.39207283A>T , CM000666.1:g.39207283A>T	GRCh37
NC_000004.10:g.38883678A>T	NCBI36
NG_031813.1:g.28260A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.817A>T MANE Select	ENSP00000382717.3:p.Asn273Tyr
ENST00000399820.7:c.817A>T	ENSP00000382717.3:p.Asn273Tyr
ENST00000503697.5:c.*285A>T	ENSP00000423706.1:n.*285A>T
ENST00000506503.1:c.817A>T	ENSP00000423491.1:p.Asn273Tyr
ENST00000506869.5:c.*398A>T	ENSP00000424319.1:n.*398A>T
ENST00000511729.5:n.41-22895A>T
ENST00000512448.1:n.411A>T
NM_025132.3:c.817A>T	NP_079408.3:p.Asn273Tyr
XM_011513724.1:c.817A>T	XP_011512026.1:p.Asn273Tyr
XM_011513725.1:c.751A>T	XP_011512027.1:p.Asn251Tyr
XM_011513726.1:c.337A>T	XP_011512028.1:p.Asn113Tyr
XM_011513727.1:c.337A>T	XP_011512029.1:p.Asn113Tyr
XM_011513728.1:c.337A>T	XP_011512030.1:p.Asn113Tyr
XM_011513729.1:c.817A>T	XP_011512031.1:p.Asn273Tyr
XR_925155.1:n.881A>T
NM_001317924.1:c.337A>T	NP_001304853.1:p.Asn113Tyr
XM_011513725.2:c.751A>T	XP_011512027.1:p.Asn251Tyr
XM_011513726.3:c.337A>T	XP_011512028.1:p.Asn113Tyr
XM_017008501.1:c.337A>T	XP_016863990.1:p.Asn113Tyr
XR_001741306.1:n.881A>T
XR_001741307.1:n.881A>T
XR_001741308.1:n.881A>T
XR_001741309.1:n.881A>T
XR_001741310.1:n.881A>T
XR_001741311.2:n.730A>T
XR_001741312.1:n.881A>T
NM_025132.4:c.817A>T MANE Select	NP_079408.3:p.Asn273Tyr
NM_001317924.2:c.337A>T	NP_001304853.1:p.Asn113Tyr