Canonical Allele Identifier: CA356638651

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39246150G>T (hg19) ; chr4:g.39244530G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244530G>T , CM000666.2:g.39244530G>T	GRCh38
NC_000004.11:g.39246150G>T , CM000666.1:g.39246150G>T	GRCh37
NC_000004.10:g.38922545G>T	NCBI36
NG_031813.1:g.67127G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2623G>T MANE Select	ENSP00000382717.3:p.Val875Phe
ENST00000399820.7:c.2623G>T	ENSP00000382717.3:p.Val875Phe
ENST00000506869.5:c.*2204G>T	ENSP00000424319.1:n.*2204G>T
ENST00000512095.5:n.1621G>T
NM_025132.3:c.2623G>T	NP_079408.3:p.Val875Phe
XM_011513724.1:c.2635G>T	XP_011512026.1:p.Val879Phe
XM_011513725.1:c.2569G>T	XP_011512027.1:p.Val857Phe
XM_011513726.1:c.2155G>T	XP_011512028.1:p.Val719Phe
XM_011513727.1:c.2155G>T	XP_011512029.1:p.Val719Phe
XM_011513728.1:c.2143G>T	XP_011512030.1:p.Val715Phe
XM_011513729.1:c.2635G>T	XP_011512031.1:p.Val879Phe
XR_925155.1:n.2699G>T
NM_001317924.1:c.2143G>T	NP_001304853.1:p.Val715Phe
XM_011513725.2:c.2569G>T	XP_011512027.1:p.Val857Phe
XM_011513726.3:c.2155G>T	XP_011512028.1:p.Val719Phe
XM_017008501.1:c.2143G>T	XP_016863990.1:p.Val715Phe
XR_001741306.1:n.2699G>T
XR_001741307.1:n.2687G>T
XR_001741308.1:n.2699G>T
XR_001741309.1:n.2687G>T
XR_001741310.1:n.2687G>T
XR_001741311.2:n.2536G>T
NM_025132.4:c.2623G>T MANE Select	NP_079408.3:p.Val875Phe
NM_001317924.2:c.2143G>T	NP_001304853.1:p.Val715Phe