Canonical Allele Identifier: CA438942001

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39245900C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244280C>A , CM000666.2:g.39244280C>A	GRCh38
NC_000004.11:g.39245900C>A , CM000666.1:g.39245900C>A	GRCh37
NC_000004.10:g.38922295C>A	NCBI36
NG_031813.1:g.66877C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.2454C>A MANE Select	ENSP00000382717.3:p.Ala818=
ENST00000399820.7:c.2454C>A	ENSP00000382717.3:p.Ala818=
ENST00000506869.5:c.*2035C>A	ENSP00000424319.1:n.*2035C>A
ENST00000512095.5:n.1452C>A
NM_025132.3:c.2454C>A	NP_079408.3:p.Ala818=
XM_011513724.1:c.2466C>A	XP_011512026.1:p.Ala822=
XM_011513725.1:c.2400C>A	XP_011512027.1:p.Ala800=
XM_011513726.1:c.1986C>A	XP_011512028.1:p.Ala662=
XM_011513727.1:c.1986C>A	XP_011512029.1:p.Ala662=
XM_011513728.1:c.1974C>A	XP_011512030.1:p.Ala658=
XM_011513729.1:c.2466C>A	XP_011512031.1:p.Ala822=
XR_925155.1:n.2530C>A
NM_001317924.1:c.1974C>A	NP_001304853.1:p.Ala658=
XM_011513725.2:c.2400C>A	XP_011512027.1:p.Ala800=
XM_011513726.3:c.1986C>A	XP_011512028.1:p.Ala662=
XM_017008501.1:c.1974C>A	XP_016863990.1:p.Ala658=
XR_001741306.1:n.2530C>A
XR_001741307.1:n.2518C>A
XR_001741308.1:n.2530C>A
XR_001741309.1:n.2518C>A
XR_001741310.1:n.2518C>A
XR_001741311.2:n.2367C>A
NM_025132.4:c.2454C>A MANE Select	NP_079408.3:p.Ala818=
NM_001317924.2:c.1974C>A	NP_001304853.1:p.Ala658=