Canonical Allele Identifier: CA95677687

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39234788G>A , CM000666.2:g.39234788G>A	GRCh38
NC_000004.11:g.39236408G>A , CM000666.1:g.39236408G>A	GRCh37
NC_000004.10:g.38912803G>A	NCBI36
NG_031813.1:g.57385G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.2276G>A MANE Select	NP_079408.3:p.Trp759Ter
ENST00000399820.8:c.2276G>A MANE Select	ENSP00000382717.3:p.Trp759Ter
NM_001317924.1:c.1796G>A	NP_001304853.1:p.Trp599Ter
NM_001317924.2:c.1796G>A	NP_001304853.1:p.Trp599Ter
NM_025132.3:c.2276G>A	NP_079408.3:p.Trp759Ter
ENST00000399820.7:c.2276G>A	ENSP00000382717.3:p.Trp759Ter
ENST00000502718.1:n.22G>A
ENST00000506869.5:c.*1857G>A	ENSP00000424319.1:n.*1857G>A
ENST00000507228.1:c.426G>A
ENST00000511729.5:n.467G>A
ENST00000512095.5:n.1274G>A
ENST00000515631.1:n.466G>A
XM_011513724.1:c.2288G>A	XP_011512026.1:p.Trp763Ter
XM_011513725.1:c.2222G>A	XP_011512027.1:p.Trp741Ter
XM_011513725.2:c.2222G>A	XP_011512027.1:p.Trp741Ter
XM_011513726.1:c.1808G>A	XP_011512028.1:p.Trp603Ter
XM_011513726.3:c.1808G>A	XP_011512028.1:p.Trp603Ter
XM_011513727.1:c.1808G>A	XP_011512029.1:p.Trp603Ter
XM_011513728.1:c.1796G>A	XP_011512030.1:p.Trp599Ter
XM_011513729.1:c.2288G>A	XP_011512031.1:p.Trp763Ter
XM_017008501.1:c.1796G>A	XP_016863990.1:p.Trp599Ter
XR_001741306.1:n.2352G>A
XR_001741307.1:n.2340G>A
XR_001741308.1:n.2352G>A
XR_001741309.1:n.2340G>A
XR_001741310.1:n.2340G>A
XR_001741311.2:n.2189G>A
XR_001741312.1:n.2376G>A
XR_925155.1:n.2352G>A