Canonical Allele Identifier: CA356630606

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39217133G>A , CM000666.2:g.39217133G>A	GRCh38
NC_000004.11:g.39218753G>A , CM000666.1:g.39218753G>A	GRCh37
NC_000004.10:g.38895148G>A	NCBI36
NG_031813.1:g.39730G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.1250-1G>A MANE Select	NP_079408.3:n.1250-1G>A
ENST00000399820.8:c.1250-1G>A MANE Select	ENSP00000382717.3:n.1250-1G>A
NM_001317924.1:c.770-1G>A	NP_001304853.1:n.770-1G>A
NM_001317924.2:c.770-1G>A	NP_001304853.1:n.770-1G>A
NM_025132.3:c.1250-1G>A	NP_079408.3:n.1250-1G>A
ENST00000399820.7:c.1250-1G>A	ENSP00000382717.3:n.1250-1G>A
ENST00000506503.1:c.1250-1G>A	ENSP00000423491.1:n.1250-1G>A
ENST00000506869.5:c.*831-1G>A	ENSP00000424319.1:n.*831-1G>A
ENST00000511729.5:n.41-11425G>A
ENST00000512095.5:n.248-1G>A
XM_011513724.1:c.1250-1G>A	XP_011512026.1:n.1250-1G>A
XM_011513725.1:c.1184-1G>A	XP_011512027.1:n.1184-1G>A
XM_011513725.2:c.1184-1G>A	XP_011512027.1:n.1184-1G>A
XM_011513726.1:c.770-1G>A	XP_011512028.1:n.770-1G>A
XM_011513726.3:c.770-1G>A	XP_011512028.1:n.770-1G>A
XM_011513727.1:c.770-1G>A	XP_011512029.1:n.770-1G>A
XM_011513728.1:c.770-1G>A	XP_011512030.1:n.770-1G>A
XM_011513729.1:c.1250-1G>A	XP_011512031.1:n.1250-1G>A
XM_017008501.1:c.770-1G>A	XP_016863990.1:n.770-1G>A
XR_001741306.1:n.1314-1G>A
XR_001741307.1:n.1314-1G>A
XR_001741308.1:n.1314-1G>A
XR_001741309.1:n.1314-1G>A
XR_001741310.1:n.1314-1G>A
XR_001741311.2:n.1163-1G>A
XR_001741312.1:n.1314-1G>A
XR_925155.1:n.1314-1G>A