Canonical Allele Identifier: CA438942003

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39245903G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244283G>A , CM000666.2:g.39244283G>A	GRCh38
NC_000004.11:g.39245903G>A , CM000666.1:g.39245903G>A	GRCh37
NC_000004.10:g.38922298G>A	NCBI36
NG_031813.1:g.66880G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2457G>A MANE Select	ENSP00000382717.3:p.Gln819=
ENST00000399820.7:c.2457G>A	ENSP00000382717.3:p.Gln819=
ENST00000506869.5:c.*2038G>A	ENSP00000424319.1:n.*2038G>A
ENST00000512095.5:n.1455G>A
NM_025132.3:c.2457G>A	NP_079408.3:p.Gln819=
XM_011513724.1:c.2469G>A	XP_011512026.1:p.Gln823=
XM_011513725.1:c.2403G>A	XP_011512027.1:p.Gln801=
XM_011513726.1:c.1989G>A	XP_011512028.1:p.Gln663=
XM_011513727.1:c.1989G>A	XP_011512029.1:p.Gln663=
XM_011513728.1:c.1977G>A	XP_011512030.1:p.Gln659=
XM_011513729.1:c.2469G>A	XP_011512031.1:p.Gln823=
XR_925155.1:n.2533G>A
NM_001317924.1:c.1977G>A	NP_001304853.1:p.Gln659=
XM_011513725.2:c.2403G>A	XP_011512027.1:p.Gln801=
XM_011513726.3:c.1989G>A	XP_011512028.1:p.Gln663=
XM_017008501.1:c.1977G>A	XP_016863990.1:p.Gln659=
XR_001741306.1:n.2533G>A
XR_001741307.1:n.2521G>A
XR_001741308.1:n.2533G>A
XR_001741309.1:n.2521G>A
XR_001741310.1:n.2521G>A
XR_001741311.2:n.2370G>A
NM_025132.4:c.2457G>A MANE Select	NP_079408.3:p.Gln819=
NM_001317924.2:c.1977G>A	NP_001304853.1:p.Gln659=