Canonical Allele Identifier: CA356638615

Gene: WDR19

Linked Data

• gnomAD v4: 4-39244522-C-T
• MyVariant Identifiers: chr4:g.39246142C>T (hg19) ; chr4:g.39244522C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244522C>T , CM000666.2:g.39244522C>T	GRCh38
NC_000004.11:g.39246142C>T , CM000666.1:g.39246142C>T	GRCh37
NC_000004.10:g.38922537C>T	NCBI36
NG_031813.1:g.67119C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2615C>T MANE Select	ENSP00000382717.3:p.Ala872Val
ENST00000399820.7:c.2615C>T	ENSP00000382717.3:p.Ala872Val
ENST00000506869.5:c.*2196C>T	ENSP00000424319.1:n.*2196C>T
ENST00000512095.5:n.1613C>T
NM_025132.3:c.2615C>T	NP_079408.3:p.Ala872Val
XM_011513724.1:c.2627C>T	XP_011512026.1:p.Ala876Val
XM_011513725.1:c.2561C>T	XP_011512027.1:p.Ala854Val
XM_011513726.1:c.2147C>T	XP_011512028.1:p.Ala716Val
XM_011513727.1:c.2147C>T	XP_011512029.1:p.Ala716Val
XM_011513728.1:c.2135C>T	XP_011512030.1:p.Ala712Val
XM_011513729.1:c.2627C>T	XP_011512031.1:p.Ala876Val
XR_925155.1:n.2691C>T
NM_001317924.1:c.2135C>T	NP_001304853.1:p.Ala712Val
XM_011513725.2:c.2561C>T	XP_011512027.1:p.Ala854Val
XM_011513726.3:c.2147C>T	XP_011512028.1:p.Ala716Val
XM_017008501.1:c.2135C>T	XP_016863990.1:p.Ala712Val
XR_001741306.1:n.2691C>T
XR_001741307.1:n.2679C>T
XR_001741308.1:n.2691C>T
XR_001741309.1:n.2679C>T
XR_001741310.1:n.2679C>T
XR_001741311.2:n.2528C>T
NM_025132.4:c.2615C>T MANE Select	NP_079408.3:p.Ala872Val
NM_001317924.2:c.2135C>T	NP_001304853.1:p.Ala712Val