Canonical Allele Identifier: CA356632893

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39228484A>C , CM000666.2:g.39228484A>C	GRCh38
NC_000004.11:g.39230104A>C , CM000666.1:g.39230104A>C	GRCh37
NC_000004.10:g.38906499A>C	NCBI36
NG_031813.1:g.51081A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.1778-2A>C MANE Select	NP_079408.3:n.1778-2A>C
ENST00000399820.8:c.1778-2A>C MANE Select	ENSP00000382717.3:n.1778-2A>C
NM_001317924.1:c.1298-2A>C	NP_001304853.1:n.1298-2A>C
NM_001317924.2:c.1298-2A>C	NP_001304853.1:n.1298-2A>C
NM_025132.3:c.1778-2A>C	NP_079408.3:n.1778-2A>C
ENST00000399820.7:c.1778-2A>C	ENSP00000382717.3:n.1778-2A>C
ENST00000506869.5:c.*1359-2A>C	ENSP00000424319.1:n.*1359-2A>C
ENST00000511729.5:n.41-74A>C
ENST00000512095.5:n.776-2A>C
XM_011513724.1:c.1778-2A>C	XP_011512026.1:n.1778-2A>C
XM_011513725.1:c.1712-2A>C	XP_011512027.1:n.1712-2A>C
XM_011513725.2:c.1712-2A>C	XP_011512027.1:n.1712-2A>C
XM_011513726.1:c.1298-2A>C	XP_011512028.1:n.1298-2A>C
XM_011513726.3:c.1298-2A>C	XP_011512028.1:n.1298-2A>C
XM_011513727.1:c.1298-2A>C	XP_011512029.1:n.1298-2A>C
XM_011513728.1:c.1298-2A>C	XP_011512030.1:n.1298-2A>C
XM_011513729.1:c.1778-2A>C	XP_011512031.1:n.1778-2A>C
XM_017008501.1:c.1298-2A>C	XP_016863990.1:n.1298-2A>C
XR_001741306.1:n.1842-2A>C
XR_001741307.1:n.1842-2A>C
XR_001741308.1:n.1842-2A>C
XR_001741309.1:n.1842-2A>C
XR_001741310.1:n.1842-2A>C
XR_001741311.2:n.1691-2A>C
XR_001741312.1:n.1842-2A>C
XR_925155.1:n.1842-2A>C