Canonical Allele Identifier: CA356631012

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39217981A>T , CM000666.2:g.39217981A>T	GRCh38
NC_000004.11:g.39219601A>T , CM000666.1:g.39219601A>T	GRCh37
NC_000004.10:g.38895996A>T	NCBI36
NG_031813.1:g.40578A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.1357-2A>T MANE Select	NP_079408.3:n.1357-2A>T
ENST00000399820.8:c.1357-2A>T MANE Select	ENSP00000382717.3:n.1357-2A>T
NM_001317924.1:c.877-2A>T	NP_001304853.1:n.877-2A>T
NM_001317924.2:c.877-2A>T	NP_001304853.1:n.877-2A>T
NM_025132.3:c.1357-2A>T	NP_079408.3:n.1357-2A>T
ENST00000399820.7:c.1357-2A>T	ENSP00000382717.3:n.1357-2A>T
ENST00000506503.1:c.1357-6A>T	ENSP00000423491.1:n.1357-6A>T
ENST00000506869.5:c.*938-2A>T	ENSP00000424319.1:n.*938-2A>T
ENST00000511729.5:n.41-10577A>T
ENST00000512095.5:n.355-2A>T
XM_011513724.1:c.1357-2A>T	XP_011512026.1:n.1357-2A>T
XM_011513725.1:c.1291-2A>T	XP_011512027.1:n.1291-2A>T
XM_011513725.2:c.1291-2A>T	XP_011512027.1:n.1291-2A>T
XM_011513726.1:c.877-2A>T	XP_011512028.1:n.877-2A>T
XM_011513726.3:c.877-2A>T	XP_011512028.1:n.877-2A>T
XM_011513727.1:c.877-2A>T	XP_011512029.1:n.877-2A>T
XM_011513728.1:c.877-2A>T	XP_011512030.1:n.877-2A>T
XM_011513729.1:c.1357-2A>T	XP_011512031.1:n.1357-2A>T
XM_017008501.1:c.877-2A>T	XP_016863990.1:n.877-2A>T
XR_001741306.1:n.1421-2A>T
XR_001741307.1:n.1421-2A>T
XR_001741308.1:n.1421-2A>T
XR_001741309.1:n.1421-2A>T
XR_001741310.1:n.1421-2A>T
XR_001741311.2:n.1270-2A>T
XR_001741312.1:n.1421-2A>T
XR_925155.1:n.1421-2A>T