Canonical Allele Identifier: CA2670361398

Gene: WDR19

Linked Data

• gnomAD v4: 4-39273080-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273080A>G , CM000666.2:g.39273080A>G	GRCh38
NC_000004.11:g.39274700A>G , CM000666.1:g.39274700A>G	GRCh37
NC_000004.10:g.38951095A>G	NCBI36
NG_031813.1:g.95677A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3565+19A>G MANE Select	ENSP00000382717.3:n.3565+19A>G
ENST00000399820.7:c.3565+19A>G	ENSP00000382717.3:n.3565+19A>G
ENST00000506869.5:c.*3146+19A>G	ENSP00000424319.1:n.*3146+19A>G
ENST00000512095.5:n.2563+19A>G
ENST00000512534.5:n.149A>G
NM_025132.3:c.3565+19A>G	NP_079408.3:n.3565+19A>G
XM_011513724.1:c.3577+19A>G	XP_011512026.1:n.3577+19A>G
XM_011513725.1:c.3511+19A>G	XP_011512027.1:n.3511+19A>G
XM_011513726.1:c.3097+19A>G	XP_011512028.1:n.3097+19A>G
XM_011513727.1:c.3097+19A>G	XP_011512029.1:n.3097+19A>G
XM_011513728.1:c.3085+19A>G	XP_011512030.1:n.3085+19A>G
XR_925155.1:n.3641+19A>G
NM_001317924.1:c.3085+19A>G	NP_001304853.1:n.3085+19A>G
XM_011513725.2:c.3511+19A>G	XP_011512027.1:n.3511+19A>G
XM_011513726.3:c.3097+19A>G	XP_011512028.1:n.3097+19A>G
XM_017008501.1:c.3085+19A>G	XP_016863990.1:n.3085+19A>G
XR_001741306.1:n.3641+19A>G
XR_001741307.1:n.3629+19A>G
XR_001741308.1:n.3641+19A>G
XR_001741309.1:n.3629+19A>G
XR_001741310.1:n.3629+19A>G
XR_001741311.2:n.3478+19A>G
NM_025132.4:c.3565+19A>G MANE Select	NP_079408.3:n.3565+19A>G
NM_001317924.2:c.3085+19A>G	NP_001304853.1:n.3085+19A>G