Canonical Allele Identifier: CA356636757

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39240275A>G , CM000666.2:g.39240275A>G	GRCh38
NC_000004.11:g.39241895A>G , CM000666.1:g.39241895A>G	GRCh37
NC_000004.10:g.38918290A>G	NCBI36
NG_031813.1:g.62872A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.2364-2A>G MANE Select	NP_079408.3:n.2364-2A>G
ENST00000399820.8:c.2364-2A>G MANE Select	ENSP00000382717.3:n.2364-2A>G
NM_001317924.1:c.1884-2A>G	NP_001304853.1:n.1884-2A>G
NM_001317924.2:c.1884-2A>G	NP_001304853.1:n.1884-2A>G
NM_025132.3:c.2364-2A>G	NP_079408.3:n.2364-2A>G
ENST00000399820.7:c.2364-2A>G	ENSP00000382717.3:n.2364-2A>G
ENST00000506869.5:c.*1945-2A>G	ENSP00000424319.1:n.*1945-2A>G
ENST00000507228.1:c.514-2A>G
ENST00000512095.5:n.1362-2A>G
XM_011513724.1:c.2376-2A>G	XP_011512026.1:n.2376-2A>G
XM_011513725.1:c.2310-2A>G	XP_011512027.1:n.2310-2A>G
XM_011513725.2:c.2310-2A>G	XP_011512027.1:n.2310-2A>G
XM_011513726.1:c.1896-2A>G	XP_011512028.1:n.1896-2A>G
XM_011513726.3:c.1896-2A>G	XP_011512028.1:n.1896-2A>G
XM_011513727.1:c.1896-2A>G	XP_011512029.1:n.1896-2A>G
XM_011513728.1:c.1884-2A>G	XP_011512030.1:n.1884-2A>G
XM_011513729.1:c.2376-2A>G	XP_011512031.1:n.2376-2A>G
XM_017008501.1:c.1884-2A>G	XP_016863990.1:n.1884-2A>G
XR_001741306.1:n.2440-2A>G
XR_001741307.1:n.2428-2A>G
XR_001741308.1:n.2440-2A>G
XR_001741309.1:n.2428-2A>G
XR_001741310.1:n.2428-2A>G
XR_001741311.2:n.2277-2A>G
XR_001741312.1:n.2464-2A>G
XR_925155.1:n.2440-2A>G