Canonical Allele Identifier: CA2891882

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39224970C>T , CM000666.2:g.39224970C>T	GRCh38
NC_000004.11:g.39226590C>T , CM000666.1:g.39226590C>T	GRCh37
NC_000004.10:g.38902985C>T	NCBI36
NG_031813.1:g.47567C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.1566C>T MANE Select	NP_079408.3:p.Pro522=
ENST00000399820.8:c.1566C>T MANE Select	ENSP00000382717.3:p.Pro522=
NM_001317924.1:c.1086C>T	NP_001304853.1:p.Pro362=
NM_001317924.2:c.1086C>T	NP_001304853.1:p.Pro362=
NM_025132.3:c.1566C>T	NP_079408.3:p.Pro522=
ENST00000399820.7:c.1566C>T	ENSP00000382717.3:p.Pro522=
ENST00000506869.5:c.*1147C>T	ENSP00000424319.1:n.*1147C>T
ENST00000511729.5:n.41-3588C>T
ENST00000512095.5:n.564C>T
XM_011513724.1:c.1566C>T	XP_011512026.1:p.Pro522=
XM_011513725.1:c.1500C>T	XP_011512027.1:p.Pro500=
XM_011513725.2:c.1500C>T	XP_011512027.1:p.Pro500=
XM_011513726.1:c.1086C>T	XP_011512028.1:p.Pro362=
XM_011513726.3:c.1086C>T	XP_011512028.1:p.Pro362=
XM_011513727.1:c.1086C>T	XP_011512029.1:p.Pro362=
XM_011513728.1:c.1086C>T	XP_011512030.1:p.Pro362=
XM_011513729.1:c.1566C>T	XP_011512031.1:p.Pro522=
XM_017008501.1:c.1086C>T	XP_016863990.1:p.Pro362=
XR_001741306.1:n.1630C>T
XR_001741307.1:n.1630C>T
XR_001741308.1:n.1630C>T
XR_001741309.1:n.1630C>T
XR_001741310.1:n.1630C>T
XR_001741311.2:n.1479C>T
XR_001741312.1:n.1630C>T
XR_925155.1:n.1630C>T