Canonical Allele Identifier: CA356647456

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39274659C>A (hg19) ; chr4:g.39273039C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273039C>A , CM000666.2:g.39273039C>A	GRCh38
NC_000004.11:g.39274659C>A , CM000666.1:g.39274659C>A	GRCh37
NC_000004.10:g.38951054C>A	NCBI36
NG_031813.1:g.95636C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3543C>A MANE Select	ENSP00000382717.3:p.Asn1181Lys
ENST00000399820.7:c.3543C>A	ENSP00000382717.3:p.Asn1181Lys
ENST00000506869.5:c.*3124C>A	ENSP00000424319.1:n.*3124C>A
ENST00000512095.5:n.2541C>A
ENST00000512534.5:n.108C>A
NM_025132.3:c.3543C>A	NP_079408.3:p.Asn1181Lys
XM_011513724.1:c.3555C>A	XP_011512026.1:p.Asn1185Lys
XM_011513725.1:c.3489C>A	XP_011512027.1:p.Asn1163Lys
XM_011513726.1:c.3075C>A	XP_011512028.1:p.Asn1025Lys
XM_011513727.1:c.3075C>A	XP_011512029.1:p.Asn1025Lys
XM_011513728.1:c.3063C>A	XP_011512030.1:p.Asn1021Lys
XR_925155.1:n.3619C>A
NM_001317924.1:c.3063C>A	NP_001304853.1:p.Asn1021Lys
XM_011513725.2:c.3489C>A	XP_011512027.1:p.Asn1163Lys
XM_011513726.3:c.3075C>A	XP_011512028.1:p.Asn1025Lys
XM_017008501.1:c.3063C>A	XP_016863990.1:p.Asn1021Lys
XR_001741306.1:n.3619C>A
XR_001741307.1:n.3607C>A
XR_001741308.1:n.3619C>A
XR_001741309.1:n.3607C>A
XR_001741310.1:n.3607C>A
XR_001741311.2:n.3456C>A
NM_025132.4:c.3543C>A MANE Select	NP_079408.3:p.Asn1181Lys
NM_001317924.2:c.3063C>A	NP_001304853.1:p.Asn1021Lys