Canonical Allele Identifier: CA356652292

Gene: WDR19

Linked Data

• gnomAD v4: 4-39277108-G-C
• MyVariant Identifiers: chr4:g.39278728G>C (hg19) ; chr4:g.39277108G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277108G>C , CM000666.2:g.39277108G>C	GRCh38
NC_000004.11:g.39278728G>C , CM000666.1:g.39278728G>C	GRCh37
NC_000004.10:g.38955123G>C	NCBI36
NG_031813.1:g.99705G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3805G>C MANE Select	ENSP00000382717.3:p.Gly1269Arg
ENST00000399820.7:c.3805G>C	ENSP00000382717.3:p.Gly1269Arg
ENST00000503733.1:n.145G>C
ENST00000506869.5:c.*3386G>C	ENSP00000424319.1:n.*3386G>C
ENST00000512534.5:n.2116G>C
ENST00000512588.5:n.147G>C
NM_025132.3:c.3805G>C	NP_079408.3:p.Gly1269Arg
XM_011513724.1:c.3817G>C	XP_011512026.1:p.Gly1273Arg
XM_011513725.1:c.3751G>C	XP_011512027.1:p.Gly1251Arg
XM_011513726.1:c.3337G>C	XP_011512028.1:p.Gly1113Arg
XM_011513727.1:c.3337G>C	XP_011512029.1:p.Gly1113Arg
XM_011513728.1:c.3325G>C	XP_011512030.1:p.Gly1109Arg
XR_925155.1:n.5515G>C
NM_001317924.1:c.3325G>C	NP_001304853.1:p.Gly1109Arg
XM_011513725.2:c.3751G>C	XP_011512027.1:p.Gly1251Arg
XM_011513726.3:c.3337G>C	XP_011512028.1:p.Gly1113Arg
XM_017008501.1:c.3325G>C	XP_016863990.1:p.Gly1109Arg
XR_001741306.1:n.4082G>C
XR_001741307.1:n.4070G>C
XR_001741308.1:n.5716G>C
XR_001741309.1:n.5503G>C
XR_001741310.1:n.5704G>C
XR_001741311.2:n.5352G>C
NM_025132.4:c.3805G>C MANE Select	NP_079408.3:p.Gly1269Arg
NM_001317924.2:c.3325G>C	NP_001304853.1:p.Gly1109Arg