Canonical Allele Identifier: CA356652253

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39278723G>T (hg19) ; chr4:g.39277103G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277103G>T , CM000666.2:g.39277103G>T	GRCh38
NC_000004.11:g.39278723G>T , CM000666.1:g.39278723G>T	GRCh37
NC_000004.10:g.38955118G>T	NCBI36
NG_031813.1:g.99700G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3800G>T MANE Select	ENSP00000382717.3:p.Cys1267Phe
ENST00000399820.7:c.3800G>T	ENSP00000382717.3:p.Cys1267Phe
ENST00000503733.1:n.140G>T
ENST00000506869.5:c.*3381G>T	ENSP00000424319.1:n.*3381G>T
ENST00000512534.5:n.2111G>T
ENST00000512588.5:n.142G>T
NM_025132.3:c.3800G>T	NP_079408.3:p.Cys1267Phe
XM_011513724.1:c.3812G>T	XP_011512026.1:p.Cys1271Phe
XM_011513725.1:c.3746G>T	XP_011512027.1:p.Cys1249Phe
XM_011513726.1:c.3332G>T	XP_011512028.1:p.Cys1111Phe
XM_011513727.1:c.3332G>T	XP_011512029.1:p.Cys1111Phe
XM_011513728.1:c.3320G>T	XP_011512030.1:p.Cys1107Phe
XR_925155.1:n.5510G>T
NM_001317924.1:c.3320G>T	NP_001304853.1:p.Cys1107Phe
XM_011513725.2:c.3746G>T	XP_011512027.1:p.Cys1249Phe
XM_011513726.3:c.3332G>T	XP_011512028.1:p.Cys1111Phe
XM_017008501.1:c.3320G>T	XP_016863990.1:p.Cys1107Phe
XR_001741306.1:n.4077G>T
XR_001741307.1:n.4065G>T
XR_001741308.1:n.5711G>T
XR_001741309.1:n.5498G>T
XR_001741310.1:n.5699G>T
XR_001741311.2:n.5347G>T
NM_025132.4:c.3800G>T MANE Select	NP_079408.3:p.Cys1267Phe
NM_001317924.2:c.3320G>T	NP_001304853.1:p.Cys1107Phe