Canonical Allele Identifier: CA438939399

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39207258T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205638T>G , CM000666.2:g.39205638T>G	GRCh38
NC_000004.11:g.39207258T>G , CM000666.1:g.39207258T>G	GRCh37
NC_000004.10:g.38883653T>G	NCBI36
NG_031813.1:g.28235T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.792T>G MANE Select	ENSP00000382717.3:p.Leu264=
ENST00000399820.7:c.792T>G	ENSP00000382717.3:p.Leu264=
ENST00000503697.5:c.*260T>G	ENSP00000423706.1:n.*260T>G
ENST00000506503.1:c.792T>G	ENSP00000423491.1:p.Leu264=
ENST00000506869.5:c.*373T>G	ENSP00000424319.1:n.*373T>G
ENST00000511729.5:n.41-22920T>G
ENST00000512448.1:n.386T>G
NM_025132.3:c.792T>G	NP_079408.3:p.Leu264=
XM_011513724.1:c.792T>G	XP_011512026.1:p.Leu264=
XM_011513725.1:c.726T>G	XP_011512027.1:p.Leu242=
XM_011513726.1:c.312T>G	XP_011512028.1:p.Leu104=
XM_011513727.1:c.312T>G	XP_011512029.1:p.Leu104=
XM_011513728.1:c.312T>G	XP_011512030.1:p.Leu104=
XM_011513729.1:c.792T>G	XP_011512031.1:p.Leu264=
XR_925155.1:n.856T>G
NM_001317924.1:c.312T>G	NP_001304853.1:p.Leu104=
XM_011513725.2:c.726T>G	XP_011512027.1:p.Leu242=
XM_011513726.3:c.312T>G	XP_011512028.1:p.Leu104=
XM_017008501.1:c.312T>G	XP_016863990.1:p.Leu104=
XR_001741306.1:n.856T>G
XR_001741307.1:n.856T>G
XR_001741308.1:n.856T>G
XR_001741309.1:n.856T>G
XR_001741310.1:n.856T>G
XR_001741311.2:n.705T>G
XR_001741312.1:n.856T>G
NM_025132.4:c.792T>G MANE Select	NP_079408.3:p.Leu264=
NM_001317924.2:c.312T>G	NP_001304853.1:p.Leu104=