Canonical Allele Identifier: CA356637303

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39245899C>T (hg19) ; chr4:g.39244279C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244279C>T , CM000666.2:g.39244279C>T	GRCh38
NC_000004.11:g.39245899C>T , CM000666.1:g.39245899C>T	GRCh37
NC_000004.10:g.38922294C>T	NCBI36
NG_031813.1:g.66876C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2453C>T MANE Select	ENSP00000382717.3:p.Ala818Val
ENST00000399820.7:c.2453C>T	ENSP00000382717.3:p.Ala818Val
ENST00000506869.5:c.*2034C>T	ENSP00000424319.1:n.*2034C>T
ENST00000512095.5:n.1451C>T
NM_025132.3:c.2453C>T	NP_079408.3:p.Ala818Val
XM_011513724.1:c.2465C>T	XP_011512026.1:p.Ala822Val
XM_011513725.1:c.2399C>T	XP_011512027.1:p.Ala800Val
XM_011513726.1:c.1985C>T	XP_011512028.1:p.Ala662Val
XM_011513727.1:c.1985C>T	XP_011512029.1:p.Ala662Val
XM_011513728.1:c.1973C>T	XP_011512030.1:p.Ala658Val
XM_011513729.1:c.2465C>T	XP_011512031.1:p.Ala822Val
XR_925155.1:n.2529C>T
NM_001317924.1:c.1973C>T	NP_001304853.1:p.Ala658Val
XM_011513725.2:c.2399C>T	XP_011512027.1:p.Ala800Val
XM_011513726.3:c.1985C>T	XP_011512028.1:p.Ala662Val
XM_017008501.1:c.1973C>T	XP_016863990.1:p.Ala658Val
XR_001741306.1:n.2529C>T
XR_001741307.1:n.2517C>T
XR_001741308.1:n.2529C>T
XR_001741309.1:n.2517C>T
XR_001741310.1:n.2517C>T
XR_001741311.2:n.2366C>T
NM_025132.4:c.2453C>T MANE Select	NP_079408.3:p.Ala818Val
NM_001317924.2:c.1973C>T	NP_001304853.1:p.Ala658Val