Canonical Allele Identifier: CA356652296

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39278728G>T (hg19) ; chr4:g.39277108G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3805G>T MANE Select	ENSP00000382717.3:p.Gly1269Ter
ENST00000399820.7:c.3805G>T	ENSP00000382717.3:p.Gly1269Ter
ENST00000503733.1:n.145G>T
ENST00000506869.5:c.*3386G>T	ENSP00000424319.1:n.*3386G>T
ENST00000512534.5:n.2116G>T
ENST00000512588.5:n.147G>T
NM_025132.3:c.3805G>T	NP_079408.3:p.Gly1269Ter
XM_011513724.1:c.3817G>T	XP_011512026.1:p.Gly1273Ter
XM_011513725.1:c.3751G>T	XP_011512027.1:p.Gly1251Ter
XM_011513726.1:c.3337G>T	XP_011512028.1:p.Gly1113Ter
XM_011513727.1:c.3337G>T	XP_011512029.1:p.Gly1113Ter
XM_011513728.1:c.3325G>T	XP_011512030.1:p.Gly1109Ter
XR_925155.1:n.5515G>T
NM_001317924.1:c.3325G>T	NP_001304853.1:p.Gly1109Ter
XM_011513725.2:c.3751G>T	XP_011512027.1:p.Gly1251Ter
XM_011513726.3:c.3337G>T	XP_011512028.1:p.Gly1113Ter
XM_017008501.1:c.3325G>T	XP_016863990.1:p.Gly1109Ter
XR_001741306.1:n.4082G>T
XR_001741307.1:n.4070G>T
XR_001741308.1:n.5716G>T
XR_001741309.1:n.5503G>T
XR_001741310.1:n.5704G>T
XR_001741311.2:n.5352G>T
NM_025132.4:c.3805G>T MANE Select	NP_079408.3:p.Gly1269Ter
NM_001317924.2:c.3325G>T	NP_001304853.1:p.Gly1109Ter