Canonical Allele Identifier: CA356638358

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39246108C>G (hg19) ; chr4:g.39244488C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244488C>G , CM000666.2:g.39244488C>G	GRCh38
NC_000004.11:g.39246108C>G , CM000666.1:g.39246108C>G	GRCh37
NC_000004.10:g.38922503C>G	NCBI36
NG_031813.1:g.67085C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.2581C>G MANE Select	ENSP00000382717.3:p.Gln861Glu
ENST00000399820.7:c.2581C>G	ENSP00000382717.3:p.Gln861Glu
ENST00000506869.5:c.*2162C>G	ENSP00000424319.1:n.*2162C>G
ENST00000512095.5:n.1579C>G
NM_025132.3:c.2581C>G	NP_079408.3:p.Gln861Glu
XM_011513724.1:c.2593C>G	XP_011512026.1:p.Gln865Glu
XM_011513725.1:c.2527C>G	XP_011512027.1:p.Gln843Glu
XM_011513726.1:c.2113C>G	XP_011512028.1:p.Gln705Glu
XM_011513727.1:c.2113C>G	XP_011512029.1:p.Gln705Glu
XM_011513728.1:c.2101C>G	XP_011512030.1:p.Gln701Glu
XM_011513729.1:c.2593C>G	XP_011512031.1:p.Gln865Glu
XR_925155.1:n.2657C>G
NM_001317924.1:c.2101C>G	NP_001304853.1:p.Gln701Glu
XM_011513725.2:c.2527C>G	XP_011512027.1:p.Gln843Glu
XM_011513726.3:c.2113C>G	XP_011512028.1:p.Gln705Glu
XM_017008501.1:c.2101C>G	XP_016863990.1:p.Gln701Glu
XR_001741306.1:n.2657C>G
XR_001741307.1:n.2645C>G
XR_001741308.1:n.2657C>G
XR_001741309.1:n.2645C>G
XR_001741310.1:n.2645C>G
XR_001741311.2:n.2494C>G
NM_025132.4:c.2581C>G MANE Select	NP_079408.3:p.Gln861Glu
NM_001317924.2:c.2101C>G	NP_001304853.1:p.Gln701Glu