Canonical Allele Identifier: CA356652317

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39278732G>T (hg19) ; chr4:g.39277112G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277112G>T , CM000666.2:g.39277112G>T	GRCh38
NC_000004.11:g.39278732G>T , CM000666.1:g.39278732G>T	GRCh37
NC_000004.10:g.38955127G>T	NCBI36
NG_031813.1:g.99709G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3809G>T MANE Select	ENSP00000382717.3:p.Cys1270Phe
ENST00000399820.7:c.3809G>T	ENSP00000382717.3:p.Cys1270Phe
ENST00000503733.1:n.149G>T
ENST00000506869.5:c.*3390G>T	ENSP00000424319.1:n.*3390G>T
ENST00000512534.5:n.2120G>T
ENST00000512588.5:n.151G>T
NM_025132.3:c.3809G>T	NP_079408.3:p.Cys1270Phe
XM_011513724.1:c.3821G>T	XP_011512026.1:p.Cys1274Phe
XM_011513725.1:c.3755G>T	XP_011512027.1:p.Cys1252Phe
XM_011513726.1:c.3341G>T	XP_011512028.1:p.Cys1114Phe
XM_011513727.1:c.3341G>T	XP_011512029.1:p.Cys1114Phe
XM_011513728.1:c.3329G>T	XP_011512030.1:p.Cys1110Phe
XR_925155.1:n.5519G>T
NM_001317924.1:c.3329G>T	NP_001304853.1:p.Cys1110Phe
XM_011513725.2:c.3755G>T	XP_011512027.1:p.Cys1252Phe
XM_011513726.3:c.3341G>T	XP_011512028.1:p.Cys1114Phe
XM_017008501.1:c.3329G>T	XP_016863990.1:p.Cys1110Phe
XR_001741306.1:n.4086G>T
XR_001741307.1:n.4074G>T
XR_001741308.1:n.5720G>T
XR_001741309.1:n.5507G>T
XR_001741310.1:n.5708G>T
XR_001741311.2:n.5356G>T
NM_025132.4:c.3809G>T MANE Select	NP_079408.3:p.Cys1270Phe
NM_001317924.2:c.3329G>T	NP_001304853.1:p.Cys1110Phe