Canonical Allele Identifier: CA438943460

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39274665C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273045C>T , CM000666.2:g.39273045C>T	GRCh38
NC_000004.11:g.39274665C>T , CM000666.1:g.39274665C>T	GRCh37
NC_000004.10:g.38951060C>T	NCBI36
NG_031813.1:g.95642C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3549C>T MANE Select	ENSP00000382717.3:p.Ile1183=
ENST00000399820.7:c.3549C>T	ENSP00000382717.3:p.Ile1183=
ENST00000506869.5:c.*3130C>T	ENSP00000424319.1:n.*3130C>T
ENST00000512095.5:n.2547C>T
ENST00000512534.5:n.114C>T
NM_025132.3:c.3549C>T	NP_079408.3:p.Ile1183=
XM_011513724.1:c.3561C>T	XP_011512026.1:p.Ile1187=
XM_011513725.1:c.3495C>T	XP_011512027.1:p.Ile1165=
XM_011513726.1:c.3081C>T	XP_011512028.1:p.Ile1027=
XM_011513727.1:c.3081C>T	XP_011512029.1:p.Ile1027=
XM_011513728.1:c.3069C>T	XP_011512030.1:p.Ile1023=
XR_925155.1:n.3625C>T
NM_001317924.1:c.3069C>T	NP_001304853.1:p.Ile1023=
XM_011513725.2:c.3495C>T	XP_011512027.1:p.Ile1165=
XM_011513726.3:c.3081C>T	XP_011512028.1:p.Ile1027=
XM_017008501.1:c.3069C>T	XP_016863990.1:p.Ile1023=
XR_001741306.1:n.3625C>T
XR_001741307.1:n.3613C>T
XR_001741308.1:n.3625C>T
XR_001741309.1:n.3613C>T
XR_001741310.1:n.3613C>T
XR_001741311.2:n.3462C>T
NM_025132.4:c.3549C>T MANE Select	NP_079408.3:p.Ile1183=
NM_001317924.2:c.3069C>T	NP_001304853.1:p.Ile1023=