Canonical Allele Identifier: CA356634194

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39233572T>G (hg19) ; chr4:g.39231952T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39231952T>G , CM000666.2:g.39231952T>G	GRCh38
NC_000004.11:g.39233572T>G , CM000666.1:g.39233572T>G	GRCh37
NC_000004.10:g.38909967T>G	NCBI36
NG_031813.1:g.54549T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.2138T>G MANE Select	ENSP00000382717.3:p.Ile713Arg
ENST00000399820.7:c.2138T>G	ENSP00000382717.3:p.Ile713Arg
ENST00000506869.5:c.*1719T>G	ENSP00000424319.1:n.*1719T>G
ENST00000507228.1:c.316T>G
ENST00000511729.5:n.329T>G
ENST00000512095.5:n.1136T>G
ENST00000515631.1:n.292T>G
NM_025132.3:c.2138T>G	NP_079408.3:p.Ile713Arg
XM_011513724.1:c.2138T>G	XP_011512026.1:p.Ile713Arg
XM_011513725.1:c.2072T>G	XP_011512027.1:p.Ile691Arg
XM_011513726.1:c.1658T>G	XP_011512028.1:p.Ile553Arg
XM_011513727.1:c.1658T>G	XP_011512029.1:p.Ile553Arg
XM_011513728.1:c.1658T>G	XP_011512030.1:p.Ile553Arg
XM_011513729.1:c.2138T>G	XP_011512031.1:p.Ile713Arg
XR_925155.1:n.2202T>G
NM_001317924.1:c.1658T>G	NP_001304853.1:p.Ile553Arg
XM_011513725.2:c.2072T>G	XP_011512027.1:p.Ile691Arg
XM_011513726.3:c.1658T>G	XP_011512028.1:p.Ile553Arg
XM_017008501.1:c.1658T>G	XP_016863990.1:p.Ile553Arg
XR_001741306.1:n.2202T>G
XR_001741307.1:n.2202T>G
XR_001741308.1:n.2202T>G
XR_001741309.1:n.2202T>G
XR_001741310.1:n.2202T>G
XR_001741311.2:n.2051T>G
XR_001741312.1:n.2202T>G
NM_025132.4:c.2138T>G MANE Select	NP_079408.3:p.Ile713Arg
NM_001317924.2:c.1658T>G	NP_001304853.1:p.Ile553Arg