Canonical Allele Identifier: CA356647475

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39274662C>G (hg19) ; chr4:g.39273042C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273042C>G , CM000666.2:g.39273042C>G	GRCh38
NC_000004.11:g.39274662C>G , CM000666.1:g.39274662C>G	GRCh37
NC_000004.10:g.38951057C>G	NCBI36
NG_031813.1:g.95639C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3546C>G MANE Select	ENSP00000382717.3:p.Asn1182Lys
ENST00000399820.7:c.3546C>G	ENSP00000382717.3:p.Asn1182Lys
ENST00000506869.5:c.*3127C>G	ENSP00000424319.1:n.*3127C>G
ENST00000512095.5:n.2544C>G
ENST00000512534.5:n.111C>G
NM_025132.3:c.3546C>G	NP_079408.3:p.Asn1182Lys
XM_011513724.1:c.3558C>G	XP_011512026.1:p.Asn1186Lys
XM_011513725.1:c.3492C>G	XP_011512027.1:p.Asn1164Lys
XM_011513726.1:c.3078C>G	XP_011512028.1:p.Asn1026Lys
XM_011513727.1:c.3078C>G	XP_011512029.1:p.Asn1026Lys
XM_011513728.1:c.3066C>G	XP_011512030.1:p.Asn1022Lys
XR_925155.1:n.3622C>G
NM_001317924.1:c.3066C>G	NP_001304853.1:p.Asn1022Lys
XM_011513725.2:c.3492C>G	XP_011512027.1:p.Asn1164Lys
XM_011513726.3:c.3078C>G	XP_011512028.1:p.Asn1026Lys
XM_017008501.1:c.3066C>G	XP_016863990.1:p.Asn1022Lys
XR_001741306.1:n.3622C>G
XR_001741307.1:n.3610C>G
XR_001741308.1:n.3622C>G
XR_001741309.1:n.3610C>G
XR_001741310.1:n.3610C>G
XR_001741311.2:n.3459C>G
NM_025132.4:c.3546C>G MANE Select	NP_079408.3:p.Asn1182Lys
NM_001317924.2:c.3066C>G	NP_001304853.1:p.Asn1022Lys