Canonical Allele Identifier: CA438943455

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39274656C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273036C>G , CM000666.2:g.39273036C>G	GRCh38
NC_000004.11:g.39274656C>G , CM000666.1:g.39274656C>G	GRCh37
NC_000004.10:g.38951051C>G	NCBI36
NG_031813.1:g.95633C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3540C>G MANE Select	ENSP00000382717.3:p.Ala1180=
ENST00000399820.7:c.3540C>G	ENSP00000382717.3:p.Ala1180=
ENST00000506869.5:c.*3121C>G	ENSP00000424319.1:n.*3121C>G
ENST00000512095.5:n.2538C>G
ENST00000512534.5:n.105C>G
NM_025132.3:c.3540C>G	NP_079408.3:p.Ala1180=
XM_011513724.1:c.3552C>G	XP_011512026.1:p.Ala1184=
XM_011513725.1:c.3486C>G	XP_011512027.1:p.Ala1162=
XM_011513726.1:c.3072C>G	XP_011512028.1:p.Ala1024=
XM_011513727.1:c.3072C>G	XP_011512029.1:p.Ala1024=
XM_011513728.1:c.3060C>G	XP_011512030.1:p.Ala1020=
XR_925155.1:n.3616C>G
NM_001317924.1:c.3060C>G	NP_001304853.1:p.Ala1020=
XM_011513725.2:c.3486C>G	XP_011512027.1:p.Ala1162=
XM_011513726.3:c.3072C>G	XP_011512028.1:p.Ala1024=
XM_017008501.1:c.3060C>G	XP_016863990.1:p.Ala1020=
XR_001741306.1:n.3616C>G
XR_001741307.1:n.3604C>G
XR_001741308.1:n.3616C>G
XR_001741309.1:n.3604C>G
XR_001741310.1:n.3604C>G
XR_001741311.2:n.3453C>G
NM_025132.4:c.3540C>G MANE Select	NP_079408.3:p.Ala1180=
NM_001317924.2:c.3060C>G	NP_001304853.1:p.Ala1020=