Canonical Allele Identifier: CA2892456

Gene: WDR19

Linked Data

• dbSNP Id: rs397786375
• ExAC: 4:39276624 G / GA
• gnomAD v2: 4-39276624-G-GA
• MyVariant Identifiers: chr4:g.39276624_39276625insA (hg19) ; chr4:g.39275004_39275005insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275004_39275005insA , CM000666.2:g.39275004_39275005insA	GRCh38
NC_000004.11:g.39276624_39276625insA , CM000666.1:g.39276624_39276625insA	GRCh37
NC_000004.10:g.38953019_38953020insA	NCBI36
NG_031813.1:g.97601_97602insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+46_3716+47insA MANE Select	ENSP00000382717.3:n.3716+46_3716+47insA
ENST00000399820.7:c.3716+46_3716+47insA	ENSP00000382717.3:n.3716+46_3716+47insA
ENST00000506869.5:c.*3297+46_*3297+47insA	ENSP00000424319.1:n.*3297+46_*3297+47insA
ENST00000512095.5:n.2760_2761insA
ENST00000512534.5:n.2027+46_2027+47insA
NM_025132.3:c.3716+46_3716+47insA	NP_079408.3:n.3716+46_3716+47insA
XM_011513724.1:c.3728+46_3728+47insA	XP_011512026.1:n.3728+46_3728+47insA
XM_011513725.1:c.3662+46_3662+47insA	XP_011512027.1:n.3662+46_3662+47insA
XM_011513726.1:c.3248+46_3248+47insA	XP_011512028.1:n.3248+46_3248+47insA
XM_011513727.1:c.3248+46_3248+47insA	XP_011512029.1:n.3248+46_3248+47insA
XM_011513728.1:c.3236+46_3236+47insA	XP_011512030.1:n.3236+46_3236+47insA
XR_925155.1:n.5426+46_5426+47insA
NM_001317924.1:c.3236+46_3236+47insA	NP_001304853.1:n.3236+46_3236+47insA
XM_011513725.2:c.3662+46_3662+47insA	XP_011512027.1:n.3662+46_3662+47insA
XM_011513726.3:c.3248+46_3248+47insA	XP_011512028.1:n.3248+46_3248+47insA
XM_017008501.1:c.3236+46_3236+47insA	XP_016863990.1:n.3236+46_3236+47insA
XR_001741306.1:n.3792+46_3792+47insA
XR_001741307.1:n.3780+46_3780+47insA
XR_001741308.1:n.5426+46_5426+47insA
XR_001741309.1:n.5414+46_5414+47insA
XR_001741310.1:n.5414+46_5414+47insA
XR_001741311.2:n.5263+46_5263+47insA
NM_025132.4:c.3716+46_3716+47insA MANE Select	NP_079408.3:n.3716+46_3716+47insA
NM_001317924.2:c.3236+46_3236+47insA	NP_001304853.1:n.3236+46_3236+47insA