Canonical Allele Identifier: CA2891893

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39225027C>G , CM000666.2:g.39225027C>G	GRCh38
NC_000004.11:g.39226647C>G , CM000666.1:g.39226647C>G	GRCh37
NC_000004.10:g.38903042C>G	NCBI36
NG_031813.1:g.47624C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.1623C>G MANE Select	NP_079408.3:p.Tyr541Ter
ENST00000399820.8:c.1623C>G MANE Select	ENSP00000382717.3:p.Tyr541Ter
NM_001317924.1:c.1143C>G	NP_001304853.1:p.Tyr381Ter
NM_001317924.2:c.1143C>G	NP_001304853.1:p.Tyr381Ter
NM_025132.3:c.1623C>G	NP_079408.3:p.Tyr541Ter
ENST00000399820.7:c.1623C>G	ENSP00000382717.3:p.Tyr541Ter
ENST00000506869.5:c.*1204C>G	ENSP00000424319.1:n.*1204C>G
ENST00000511729.5:n.41-3531C>G
ENST00000512095.5:n.621C>G
XM_011513724.1:c.1623C>G	XP_011512026.1:p.Tyr541Ter
XM_011513725.1:c.1557C>G	XP_011512027.1:p.Tyr519Ter
XM_011513725.2:c.1557C>G	XP_011512027.1:p.Tyr519Ter
XM_011513726.1:c.1143C>G	XP_011512028.1:p.Tyr381Ter
XM_011513726.3:c.1143C>G	XP_011512028.1:p.Tyr381Ter
XM_011513727.1:c.1143C>G	XP_011512029.1:p.Tyr381Ter
XM_011513728.1:c.1143C>G	XP_011512030.1:p.Tyr381Ter
XM_011513729.1:c.1623C>G	XP_011512031.1:p.Tyr541Ter
XM_017008501.1:c.1143C>G	XP_016863990.1:p.Tyr381Ter
XR_001741306.1:n.1687C>G
XR_001741307.1:n.1687C>G
XR_001741308.1:n.1687C>G
XR_001741309.1:n.1687C>G
XR_001741310.1:n.1687C>G
XR_001741311.2:n.1536C>G
XR_001741312.1:n.1687C>G
XR_925155.1:n.1687C>G