Canonical Allele Identifier: CA2761116426

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275049_39275050insAGAG , CM000666.2:g.39275049_39275050insAGAG	GRCh38
NC_000004.11:g.39276669_39276670insAGAG , CM000666.1:g.39276669_39276670insAGAG	GRCh37
NC_000004.10:g.38953064_38953065insAGAG	NCBI36
NG_031813.1:g.97646_97647insAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+91_3716+92insAGAG MANE Select	ENSP00000382717.3:n.3716+91_3716+92insAGAG
ENST00000399820.7:c.3716+91_3716+92insAGAG	ENSP00000382717.3:n.3716+91_3716+92insAGAG
ENST00000506869.5:c.*3297+91_*3297+92insAGAG	ENSP00000424319.1:n.*3297+91_*3297+92insAGAG
ENST00000512095.5:n.2805_2806insAGAG
ENST00000512534.5:n.2027+91_2027+92insAGAG
NM_025132.3:c.3716+91_3716+92insAGAG	NP_079408.3:n.3716+91_3716+92insAGAG
XM_011513724.1:c.3728+91_3728+92insAGAG	XP_011512026.1:n.3728+91_3728+92insAGAG
XM_011513725.1:c.3662+91_3662+92insAGAG	XP_011512027.1:n.3662+91_3662+92insAGAG
XM_011513726.1:c.3248+91_3248+92insAGAG	XP_011512028.1:n.3248+91_3248+92insAGAG
XM_011513727.1:c.3248+91_3248+92insAGAG	XP_011512029.1:n.3248+91_3248+92insAGAG
XM_011513728.1:c.3236+91_3236+92insAGAG	XP_011512030.1:n.3236+91_3236+92insAGAG
XR_925155.1:n.5426+91_5426+92insAGAG
NM_001317924.1:c.3236+91_3236+92insAGAG	NP_001304853.1:n.3236+91_3236+92insAGAG
XM_011513725.2:c.3662+91_3662+92insAGAG	XP_011512027.1:n.3662+91_3662+92insAGAG
XM_011513726.3:c.3248+91_3248+92insAGAG	XP_011512028.1:n.3248+91_3248+92insAGAG
XM_017008501.1:c.3236+91_3236+92insAGAG	XP_016863990.1:n.3236+91_3236+92insAGAG
XR_001741306.1:n.3792+91_3792+92insAGAG
XR_001741307.1:n.3780+91_3780+92insAGAG
XR_001741308.1:n.5426+91_5426+92insAGAG
XR_001741309.1:n.5414+91_5414+92insAGAG
XR_001741310.1:n.5414+91_5414+92insAGAG
XR_001741311.2:n.5263+91_5263+92insAGAG
NM_025132.4:c.3716+91_3716+92insAGAG MANE Select	NP_079408.3:n.3716+91_3716+92insAGAG
NM_001317924.2:c.3236+91_3236+92insAGAG	NP_001304853.1:n.3236+91_3236+92insAGAG