Canonical Allele Identifier: CA356637500

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39245989C>A (hg19) ; chr4:g.39244369C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244369C>A , CM000666.2:g.39244369C>A	GRCh38
NC_000004.11:g.39245989C>A , CM000666.1:g.39245989C>A	GRCh37
NC_000004.10:g.38922384C>A	NCBI36
NG_031813.1:g.66966C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2543C>A MANE Select	ENSP00000382717.3:p.Ala848Asp
ENST00000399820.7:c.2543C>A	ENSP00000382717.3:p.Ala848Asp
ENST00000506869.5:c.*2124C>A	ENSP00000424319.1:n.*2124C>A
ENST00000512095.5:n.1541C>A
NM_025132.3:c.2543C>A	NP_079408.3:p.Ala848Asp
XM_011513724.1:c.2555C>A	XP_011512026.1:p.Ala852Asp
XM_011513725.1:c.2489C>A	XP_011512027.1:p.Ala830Asp
XM_011513726.1:c.2075C>A	XP_011512028.1:p.Ala692Asp
XM_011513727.1:c.2075C>A	XP_011512029.1:p.Ala692Asp
XM_011513728.1:c.2063C>A	XP_011512030.1:p.Ala688Asp
XM_011513729.1:c.2555C>A	XP_011512031.1:p.Ala852Asp
XR_925155.1:n.2619C>A
NM_001317924.1:c.2063C>A	NP_001304853.1:p.Ala688Asp
XM_011513725.2:c.2489C>A	XP_011512027.1:p.Ala830Asp
XM_011513726.3:c.2075C>A	XP_011512028.1:p.Ala692Asp
XM_017008501.1:c.2063C>A	XP_016863990.1:p.Ala688Asp
XR_001741306.1:n.2619C>A
XR_001741307.1:n.2607C>A
XR_001741308.1:n.2619C>A
XR_001741309.1:n.2607C>A
XR_001741310.1:n.2607C>A
XR_001741311.2:n.2456C>A
NM_025132.4:c.2543C>A MANE Select	NP_079408.3:p.Ala848Asp
NM_001317924.2:c.2063C>A	NP_001304853.1:p.Ala688Asp