Canonical Allele Identifier: CA95703876

Gene: WDR19

Linked Data

• dbSNP Id: rs869241655
• MyVariant Identifiers: chr4:g.39276625_39276626insG (hg19) ; chr4:g.39275005_39275006insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275005_39275006insG , CM000666.2:g.39275005_39275006insG	GRCh38
NC_000004.11:g.39276625_39276626insG , CM000666.1:g.39276625_39276626insG	GRCh37
NC_000004.10:g.38953020_38953021insG	NCBI36
NG_031813.1:g.97602_97603insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+47_3716+48insG MANE Select	ENSP00000382717.3:n.3716+47_3716+48insG
ENST00000399820.7:c.3716+47_3716+48insG	ENSP00000382717.3:n.3716+47_3716+48insG
ENST00000506869.5:c.*3297+47_*3297+48insG	ENSP00000424319.1:n.*3297+47_*3297+48insG
ENST00000512095.5:n.2761_2762insG
ENST00000512534.5:n.2027+47_2027+48insG
NM_025132.3:c.3716+47_3716+48insG	NP_079408.3:n.3716+47_3716+48insG
XM_011513724.1:c.3728+47_3728+48insG	XP_011512026.1:n.3728+47_3728+48insG
XM_011513725.1:c.3662+47_3662+48insG	XP_011512027.1:n.3662+47_3662+48insG
XM_011513726.1:c.3248+47_3248+48insG	XP_011512028.1:n.3248+47_3248+48insG
XM_011513727.1:c.3248+47_3248+48insG	XP_011512029.1:n.3248+47_3248+48insG
XM_011513728.1:c.3236+47_3236+48insG	XP_011512030.1:n.3236+47_3236+48insG
XR_925155.1:n.5426+47_5426+48insG
NM_001317924.1:c.3236+47_3236+48insG	NP_001304853.1:n.3236+47_3236+48insG
XM_011513725.2:c.3662+47_3662+48insG	XP_011512027.1:n.3662+47_3662+48insG
XM_011513726.3:c.3248+47_3248+48insG	XP_011512028.1:n.3248+47_3248+48insG
XM_017008501.1:c.3236+47_3236+48insG	XP_016863990.1:n.3236+47_3236+48insG
XR_001741306.1:n.3792+47_3792+48insG
XR_001741307.1:n.3780+47_3780+48insG
XR_001741308.1:n.5426+47_5426+48insG
XR_001741309.1:n.5414+47_5414+48insG
XR_001741310.1:n.5414+47_5414+48insG
XR_001741311.2:n.5263+47_5263+48insG
NM_025132.4:c.3716+47_3716+48insG MANE Select	NP_079408.3:n.3716+47_3716+48insG
NM_001317924.2:c.3236+47_3236+48insG	NP_001304853.1:n.3236+47_3236+48insG