Canonical Allele Identifier: CA356637521

Gene: WDR19

Linked Data

• dbSNP Id: rs1332458650
• gnomAD v3: 4-39244379-G-T
• gnomAD v4: 4-39244379-G-T
• MyVariant Identifiers: chr4:g.39245999G>T (hg19) ; chr4:g.39244379G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244379G>T , CM000666.2:g.39244379G>T	GRCh38
NC_000004.11:g.39245999G>T , CM000666.1:g.39245999G>T	GRCh37
NC_000004.10:g.38922394G>T	NCBI36
NG_031813.1:g.66976G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.2553G>T MANE Select	ENSP00000382717.3:p.Glu851Asp
ENST00000399820.7:c.2553G>T	ENSP00000382717.3:p.Glu851Asp
ENST00000506869.5:c.*2134G>T	ENSP00000424319.1:n.*2134G>T
ENST00000512095.5:n.1551G>T
NM_025132.3:c.2553G>T	NP_079408.3:p.Glu851Asp
XM_011513724.1:c.2565G>T	XP_011512026.1:p.Glu855Asp
XM_011513725.1:c.2499G>T	XP_011512027.1:p.Glu833Asp
XM_011513726.1:c.2085G>T	XP_011512028.1:p.Glu695Asp
XM_011513727.1:c.2085G>T	XP_011512029.1:p.Glu695Asp
XM_011513728.1:c.2073G>T	XP_011512030.1:p.Glu691Asp
XM_011513729.1:c.2565G>T	XP_011512031.1:p.Glu855Asp
XR_925155.1:n.2629G>T
NM_001317924.1:c.2073G>T	NP_001304853.1:p.Glu691Asp
XM_011513725.2:c.2499G>T	XP_011512027.1:p.Glu833Asp
XM_011513726.3:c.2085G>T	XP_011512028.1:p.Glu695Asp
XM_017008501.1:c.2073G>T	XP_016863990.1:p.Glu691Asp
XR_001741306.1:n.2629G>T
XR_001741307.1:n.2617G>T
XR_001741308.1:n.2629G>T
XR_001741309.1:n.2617G>T
XR_001741310.1:n.2617G>T
XR_001741311.2:n.2466G>T
NM_025132.4:c.2553G>T MANE Select	NP_079408.3:p.Glu851Asp
NM_001317924.2:c.2073G>T	NP_001304853.1:p.Glu691Asp