Canonical Allele Identifier: CA2892383

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39270119C>G , CM000666.2:g.39270119C>G	GRCh38
NC_000004.11:g.39271739C>G , CM000666.1:g.39271739C>G	GRCh37
NC_000004.10:g.38948134C>G	NCBI36
NG_031813.1:g.92716C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.3483+19C>G MANE Select	NP_079408.3:n.3483+19C>G
ENST00000399820.8:c.3483+19C>G MANE Select	ENSP00000382717.3:n.3483+19C>G
NM_001317924.1:c.3003+19C>G	NP_001304853.1:n.3003+19C>G
NM_001317924.2:c.3003+19C>G	NP_001304853.1:n.3003+19C>G
NM_025132.3:c.3483+19C>G	NP_079408.3:n.3483+19C>G
ENST00000399820.7:c.3483+19C>G	ENSP00000382717.3:n.3483+19C>G
ENST00000506869.5:c.*3064+19C>G	ENSP00000424319.1:n.*3064+19C>G
ENST00000512095.5:n.2481+19C>G
ENST00000512534.5:n.48+19C>G
XM_011513724.1:c.3495+19C>G	XP_011512026.1:n.3495+19C>G
XM_011513725.1:c.3429+19C>G	XP_011512027.1:n.3429+19C>G
XM_011513725.2:c.3429+19C>G	XP_011512027.1:n.3429+19C>G
XM_011513726.1:c.3015+19C>G	XP_011512028.1:n.3015+19C>G
XM_011513726.3:c.3015+19C>G	XP_011512028.1:n.3015+19C>G
XM_011513727.1:c.3015+19C>G	XP_011512029.1:n.3015+19C>G
XM_011513728.1:c.3003+19C>G	XP_011512030.1:n.3003+19C>G
XM_017008501.1:c.3003+19C>G	XP_016863990.1:n.3003+19C>G
XR_001741306.1:n.3559+19C>G
XR_001741307.1:n.3547+19C>G
XR_001741308.1:n.3559+19C>G
XR_001741309.1:n.3547+19C>G
XR_001741310.1:n.3547+19C>G
XR_001741311.2:n.3396+19C>G
XR_925155.1:n.3559+19C>G