Canonical Allele Identifier: CA356647346

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39274640T>A (hg19) ; chr4:g.39273020T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273020T>A , CM000666.2:g.39273020T>A	GRCh38
NC_000004.11:g.39274640T>A , CM000666.1:g.39274640T>A	GRCh37
NC_000004.10:g.38951035T>A	NCBI36
NG_031813.1:g.95617T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3524T>A MANE Select	ENSP00000382717.3:p.Met1175Lys
ENST00000399820.7:c.3524T>A	ENSP00000382717.3:p.Met1175Lys
ENST00000506869.5:c.*3105T>A	ENSP00000424319.1:n.*3105T>A
ENST00000512095.5:n.2522T>A
ENST00000512534.5:n.89T>A
NM_025132.3:c.3524T>A	NP_079408.3:p.Met1175Lys
XM_011513724.1:c.3536T>A	XP_011512026.1:p.Met1179Lys
XM_011513725.1:c.3470T>A	XP_011512027.1:p.Met1157Lys
XM_011513726.1:c.3056T>A	XP_011512028.1:p.Met1019Lys
XM_011513727.1:c.3056T>A	XP_011512029.1:p.Met1019Lys
XM_011513728.1:c.3044T>A	XP_011512030.1:p.Met1015Lys
XR_925155.1:n.3600T>A
NM_001317924.1:c.3044T>A	NP_001304853.1:p.Met1015Lys
XM_011513725.2:c.3470T>A	XP_011512027.1:p.Met1157Lys
XM_011513726.3:c.3056T>A	XP_011512028.1:p.Met1019Lys
XM_017008501.1:c.3044T>A	XP_016863990.1:p.Met1015Lys
XR_001741306.1:n.3600T>A
XR_001741307.1:n.3588T>A
XR_001741308.1:n.3600T>A
XR_001741309.1:n.3588T>A
XR_001741310.1:n.3588T>A
XR_001741311.2:n.3437T>A
NM_025132.4:c.3524T>A MANE Select	NP_079408.3:p.Met1175Lys
NM_001317924.2:c.3044T>A	NP_001304853.1:p.Met1015Lys