Canonical Allele Identifier: CA438939397

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39207252A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205632A>T , CM000666.2:g.39205632A>T	GRCh38
NC_000004.11:g.39207252A>T , CM000666.1:g.39207252A>T	GRCh37
NC_000004.10:g.38883647A>T	NCBI36
NG_031813.1:g.28229A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.786A>T MANE Select	ENSP00000382717.3:p.Gly262=
ENST00000399820.7:c.786A>T	ENSP00000382717.3:p.Gly262=
ENST00000503697.5:c.*254A>T	ENSP00000423706.1:n.*254A>T
ENST00000506503.1:c.786A>T	ENSP00000423491.1:p.Gly262=
ENST00000506869.5:c.*367A>T	ENSP00000424319.1:n.*367A>T
ENST00000511729.5:n.41-22926A>T
ENST00000512448.1:n.380A>T
NM_025132.3:c.786A>T	NP_079408.3:p.Gly262=
XM_011513724.1:c.786A>T	XP_011512026.1:p.Gly262=
XM_011513725.1:c.720A>T	XP_011512027.1:p.Gly240=
XM_011513726.1:c.306A>T	XP_011512028.1:p.Gly102=
XM_011513727.1:c.306A>T	XP_011512029.1:p.Gly102=
XM_011513728.1:c.306A>T	XP_011512030.1:p.Gly102=
XM_011513729.1:c.786A>T	XP_011512031.1:p.Gly262=
XR_925155.1:n.850A>T
NM_001317924.1:c.306A>T	NP_001304853.1:p.Gly102=
XM_011513725.2:c.720A>T	XP_011512027.1:p.Gly240=
XM_011513726.3:c.306A>T	XP_011512028.1:p.Gly102=
XM_017008501.1:c.306A>T	XP_016863990.1:p.Gly102=
XR_001741306.1:n.850A>T
XR_001741307.1:n.850A>T
XR_001741308.1:n.850A>T
XR_001741309.1:n.850A>T
XR_001741310.1:n.850A>T
XR_001741311.2:n.699A>T
XR_001741312.1:n.850A>T
NM_025132.4:c.786A>T MANE Select	NP_079408.3:p.Gly262=
NM_001317924.2:c.306A>T	NP_001304853.1:p.Gly102=