Canonical Allele Identifier: CA1452057035

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275053_39275054delinsTG , CM000666.2:g.39275053_39275054delinsTG	GRCh38
NC_000004.11:g.39276673_39276674delinsTG , CM000666.1:g.39276673_39276674delinsTG	GRCh37
NC_000004.10:g.38953068_38953069delinsTG	NCBI36
NG_031813.1:g.97650_97651delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+95_3716+96delinsTG MANE Select	ENSP00000382717.3:n.3716+95_3716+96delinsTG
ENST00000399820.7:c.3716+95_3716+96delinsTG	ENSP00000382717.3:n.3716+95_3716+96delinsTG
ENST00000506869.5:c.*3297+95_*3297+96delinsTG	ENSP00000424319.1:n.*3297+95_*3297+96delinsTG
ENST00000512095.5:n.2809_2810delinsTG
ENST00000512534.5:n.2027+95_2027+96delinsTG
NM_025132.3:c.3716+95_3716+96delinsTG	NP_079408.3:n.3716+95_3716+96delinsTG
XM_011513724.1:c.3728+95_3728+96delinsTG	XP_011512026.1:n.3728+95_3728+96delinsTG
XM_011513725.1:c.3662+95_3662+96delinsTG	XP_011512027.1:n.3662+95_3662+96delinsTG
XM_011513726.1:c.3248+95_3248+96delinsTG	XP_011512028.1:n.3248+95_3248+96delinsTG
XM_011513727.1:c.3248+95_3248+96delinsTG	XP_011512029.1:n.3248+95_3248+96delinsTG
XM_011513728.1:c.3236+95_3236+96delinsTG	XP_011512030.1:n.3236+95_3236+96delinsTG
XR_925155.1:n.5426+95_5426+96delinsTG
NM_001317924.1:c.3236+95_3236+96delinsTG	NP_001304853.1:n.3236+95_3236+96delinsTG
XM_011513725.2:c.3662+95_3662+96delinsTG	XP_011512027.1:n.3662+95_3662+96delinsTG
XM_011513726.3:c.3248+95_3248+96delinsTG	XP_011512028.1:n.3248+95_3248+96delinsTG
XM_017008501.1:c.3236+95_3236+96delinsTG	XP_016863990.1:n.3236+95_3236+96delinsTG
XR_001741306.1:n.3792+95_3792+96delinsTG
XR_001741307.1:n.3780+95_3780+96delinsTG
XR_001741308.1:n.5426+95_5426+96delinsTG
XR_001741309.1:n.5414+95_5414+96delinsTG
XR_001741310.1:n.5414+95_5414+96delinsTG
XR_001741311.2:n.5263+95_5263+96delinsTG
NM_025132.4:c.3716+95_3716+96delinsTG MANE Select	NP_079408.3:n.3716+95_3716+96delinsTG
NM_001317924.2:c.3236+95_3236+96delinsTG	NP_001304853.1:n.3236+95_3236+96delinsTG