Canonical Allele Identifier: CA1451994801

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205670_39205672delinsAAG , CM000666.2:g.39205670_39205672delinsAAG	GRCh38
NC_000004.11:g.39207290_39207292delinsAAG , CM000666.1:g.39207290_39207292delinsAAG	GRCh37
NC_000004.10:g.38883685_38883687delinsAAG	NCBI36
NG_031813.1:g.28267_28269delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.824_826delinsAAG MANE Select	ENSP00000382717.3:p.Lys275=
ENST00000399820.7:c.824_826delinsAAG	ENSP00000382717.3:p.Lys275=
ENST00000503697.5:c.*292_*294delinsAAG	ENSP00000423706.1:n.*292_*294delinsAAG
ENST00000506503.1:c.824_826delinsAAG	ENSP00000423491.1:p.Lys275=
ENST00000506869.5:c.*405_*407delinsAAG	ENSP00000424319.1:n.*405_*407delinsAAG
ENST00000511729.5:n.41-22888_41-22886delinsAAG
ENST00000512448.1:n.418_420delinsAAG
NM_025132.3:c.824_826delinsAAG	NP_079408.3:p.Lys275=
XM_011513724.1:c.824_826delinsAAG	XP_011512026.1:p.Lys275=
XM_011513725.1:c.758_760delinsAAG	XP_011512027.1:p.Lys253=
XM_011513726.1:c.344_346delinsAAG	XP_011512028.1:p.Lys115=
XM_011513727.1:c.344_346delinsAAG	XP_011512029.1:p.Lys115=
XM_011513728.1:c.344_346delinsAAG	XP_011512030.1:p.Lys115=
XM_011513729.1:c.824_826delinsAAG	XP_011512031.1:p.Lys275=
XR_925155.1:n.888_890delinsAAG
NM_001317924.1:c.344_346delinsAAG	NP_001304853.1:p.Lys115=
XM_011513725.2:c.758_760delinsAAG	XP_011512027.1:p.Lys253=
XM_011513726.3:c.344_346delinsAAG	XP_011512028.1:p.Lys115=
XM_017008501.1:c.344_346delinsAAG	XP_016863990.1:p.Lys115=
XR_001741306.1:n.888_890delinsAAG
XR_001741307.1:n.888_890delinsAAG
XR_001741308.1:n.888_890delinsAAG
XR_001741309.1:n.888_890delinsAAG
XR_001741310.1:n.888_890delinsAAG
XR_001741311.2:n.737_739delinsAAG
XR_001741312.1:n.888_890delinsAAG
NM_025132.4:c.824_826delinsAAG MANE Select	NP_079408.3:p.Lys275=
NM_001317924.2:c.344_346delinsAAG	NP_001304853.1:p.Lys115=