Canonical Allele Identifier: CA438943857

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39276576C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39274956C>T , CM000666.2:g.39274956C>T	GRCh38
NC_000004.11:g.39276576C>T , CM000666.1:g.39276576C>T	GRCh37
NC_000004.10:g.38952971C>T	NCBI36
NG_031813.1:g.97553C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3714C>T MANE Select	ENSP00000382717.3:p.Val1238=
ENST00000399820.7:c.3714C>T	ENSP00000382717.3:p.Val1238=
ENST00000506869.5:c.*3295C>T	ENSP00000424319.1:n.*3295C>T
ENST00000512095.5:n.2712C>T
ENST00000512534.5:n.2025C>T
NM_025132.3:c.3714C>T	NP_079408.3:p.Val1238=
XM_011513724.1:c.3726C>T	XP_011512026.1:p.Val1242=
XM_011513725.1:c.3660C>T	XP_011512027.1:p.Val1220=
XM_011513726.1:c.3246C>T	XP_011512028.1:p.Val1082=
XM_011513727.1:c.3246C>T	XP_011512029.1:p.Val1082=
XM_011513728.1:c.3234C>T	XP_011512030.1:p.Val1078=
XR_925155.1:n.5424C>T
NM_001317924.1:c.3234C>T	NP_001304853.1:p.Val1078=
XM_011513725.2:c.3660C>T	XP_011512027.1:p.Val1220=
XM_011513726.3:c.3246C>T	XP_011512028.1:p.Val1082=
XM_017008501.1:c.3234C>T	XP_016863990.1:p.Val1078=
XR_001741306.1:n.3790C>T
XR_001741307.1:n.3778C>T
XR_001741308.1:n.5424C>T
XR_001741309.1:n.5412C>T
XR_001741310.1:n.5412C>T
XR_001741311.2:n.5261C>T
NM_025132.4:c.3714C>T MANE Select	NP_079408.3:p.Val1238=
NM_001317924.2:c.3234C>T	NP_001304853.1:p.Val1078=