Canonical Allele Identifier: CA2892521

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39278222C>T , CM000666.2:g.39278222C>T	GRCh38
NC_000004.11:g.39279842C>T , CM000666.1:g.39279842C>T	GRCh37
NC_000004.10:g.38956237C>T	NCBI36
NG_031813.1:g.100819C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3917+15C>T MANE Select	ENSP00000382717.3:n.3917+15C>T
ENST00000399820.7:c.3917+15C>T	ENSP00000382717.3:n.3917+15C>T
ENST00000503733.1:n.272+15C>T
ENST00000506869.5:c.*3498+15C>T	ENSP00000424319.1:n.*3498+15C>T
ENST00000512534.5:n.2228+15C>T
ENST00000512588.5:n.259+15C>T
NM_025132.3:c.3917+15C>T	NP_079408.3:n.3917+15C>T
XM_011513724.1:c.3929+15C>T	XP_011512026.1:n.3929+15C>T
XM_011513725.1:c.3863+15C>T	XP_011512027.1:n.3863+15C>T
XM_011513726.1:c.3449+15C>T	XP_011512028.1:n.3449+15C>T
XM_011513727.1:c.3449+15C>T	XP_011512029.1:n.3449+15C>T
XM_011513728.1:c.3437+15C>T	XP_011512030.1:n.3437+15C>T
XR_925155.1:n.5627+15C>T
NM_001317924.1:c.3437+15C>T	NP_001304853.1:n.3437+15C>T
XM_011513725.2:c.3863+15C>T	XP_011512027.1:n.3863+15C>T
XM_011513726.3:c.3449+15C>T	XP_011512028.1:n.3449+15C>T
XM_017008501.1:c.3437+15C>T	XP_016863990.1:n.3437+15C>T
XR_001741306.1:n.4194+15C>T
XR_001741307.1:n.4182+15C>T
XR_001741308.1:n.5828+15C>T
XR_001741309.1:n.5615+15C>T
XR_001741310.1:n.5816+15C>T
XR_001741311.2:n.5464+15C>T
NM_025132.4:c.3917+15C>T MANE Select	NP_079408.3:n.3917+15C>T
NM_001317924.2:c.3437+15C>T	NP_001304853.1:n.3437+15C>T