Canonical Allele Identifier: CA2891607

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39194641C>T , CM000666.2:g.39194641C>T	GRCh38
NC_000004.11:g.39196261C>T , CM000666.1:g.39196261C>T	GRCh37
NC_000004.10:g.38872656C>T	NCBI36
NG_031813.1:g.17238C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.388C>T MANE Select	NP_079408.3:p.Arg130Ter
ENST00000399820.8:c.388C>T MANE Select	ENSP00000382717.3:p.Arg130Ter
NM_001317924.1:c.-74-4837C>T	NP_001304853.1:n.-74-4837C>T
NM_001317924.2:c.-74-4837C>T	NP_001304853.1:n.-74-4837C>T
NM_025132.3:c.388C>T	NP_079408.3:p.Arg130Ter
ENST00000399820.7:c.388C>T	ENSP00000382717.3:p.Arg130Ter
ENST00000502389.1:n.415C>T
ENST00000503697.5:c.290+4860C>T	ENSP00000423706.1:n.290+4860C>T
ENST00000505055.5:c.225-4837C>T	ENSP00000425949.1:n.225-4837C>T
ENST00000506503.1:c.388C>T	ENSP00000423491.1:p.Arg130Ter
ENST00000506869.5:c.291-4837C>T	ENSP00000424319.1:n.291-4837C>T
ENST00000509560.5:c.211C>T	ENSP00000426918.1:p.Arg71Ter
ENST00000511729.5:n.40+12078C>T
ENST00000512112.5:c.-74-4837C>T	ENSP00000421888.1:n.-74-4837C>T
XM_011513724.1:c.388C>T	XP_011512026.1:p.Arg130Ter
XM_011513725.1:c.322C>T	XP_011512027.1:p.Arg108Ter
XM_011513725.2:c.322C>T	XP_011512027.1:p.Arg108Ter
XM_011513726.1:c.-74-4837C>T	XP_011512028.1:n.-74-4837C>T
XM_011513726.3:c.-74-4837C>T	XP_011512028.1:n.-74-4837C>T
XM_011513727.1:c.-74-4837C>T	XP_011512029.1:n.-74-4837C>T
XM_011513728.1:c.-74-4837C>T	XP_011512030.1:n.-74-4837C>T
XM_011513729.1:c.388C>T	XP_011512031.1:p.Arg130Ter
XM_017008501.1:c.-74-4837C>T	XP_016863990.1:n.-74-4837C>T
XR_001741306.1:n.452C>T
XR_001741307.1:n.452C>T
XR_001741308.1:n.452C>T
XR_001741309.1:n.452C>T
XR_001741310.1:n.452C>T
XR_001741311.2:n.320-4837C>T
XR_001741312.1:n.452C>T
XR_925155.1:n.452C>T