Canonical Allele Identifier: CA2670359583
Gene: WDR19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39244416_39244417insACATAATT , CM000666.2:g.39244416_39244417insACATAATT GRCh38
NC_000004.11:g.39246036_39246037insACATAATT , CM000666.1:g.39246036_39246037insACATAATT GRCh37
NC_000004.10:g.38922431_38922432insACATAATT NCBI36
NG_031813.1:g.67013_67014insACATAATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000399820.8:c.2562+28_2562+29insACATAATT MANE Select ENSP00000382717.3:n.2562+28_2562+29insACATAATT
ENST00000399820.7:c.2562+28_2562+29insACATAATT ENSP00000382717.3:n.2562+28_2562+29insACATAATT
ENST00000506869.5:c.*2143+28_*2143+29insACATAATT ENSP00000424319.1:n.*2143+28_*2143+29insACATAATT
ENST00000512095.5:n.1560+28_1560+29insACATAATT
NM_025132.3:c.2562+28_2562+29insACATAATT NP_079408.3:n.2562+28_2562+29insACATAATT
XM_011513724.1:c.2574+28_2574+29insACATAATT XP_011512026.1:n.2574+28_2574+29insACATAATT
XM_011513725.1:c.2508+28_2508+29insACATAATT XP_011512027.1:n.2508+28_2508+29insACATAATT
XM_011513726.1:c.2094+28_2094+29insACATAATT XP_011512028.1:n.2094+28_2094+29insACATAATT
XM_011513727.1:c.2094+28_2094+29insACATAATT XP_011512029.1:n.2094+28_2094+29insACATAATT
XM_011513728.1:c.2082+28_2082+29insACATAATT XP_011512030.1:n.2082+28_2082+29insACATAATT
XM_011513729.1:c.2574+28_2574+29insACATAATT XP_011512031.1:n.2574+28_2574+29insACATAATT
XR_925155.1:n.2638+28_2638+29insACATAATT
NM_001317924.1:c.2082+28_2082+29insACATAATT NP_001304853.1:n.2082+28_2082+29insACATAATT
XM_011513725.2:c.2508+28_2508+29insACATAATT XP_011512027.1:n.2508+28_2508+29insACATAATT
XM_011513726.3:c.2094+28_2094+29insACATAATT XP_011512028.1:n.2094+28_2094+29insACATAATT
XM_017008501.1:c.2082+28_2082+29insACATAATT XP_016863990.1:n.2082+28_2082+29insACATAATT
XR_001741306.1:n.2638+28_2638+29insACATAATT
XR_001741307.1:n.2626+28_2626+29insACATAATT
XR_001741308.1:n.2638+28_2638+29insACATAATT
XR_001741309.1:n.2626+28_2626+29insACATAATT
XR_001741310.1:n.2626+28_2626+29insACATAATT
XR_001741311.2:n.2475+28_2475+29insACATAATT
NM_025132.4:c.2562+28_2562+29insACATAATT MANE Select NP_079408.3:n.2562+28_2562+29insACATAATT
NM_001317924.2:c.2082+28_2082+29insACATAATT NP_001304853.1:n.2082+28_2082+29insACATAATT