Canonical Allele Identifier: CA2580101963
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 88978
ClinVar RCV Id: RCV000074476
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41860544_41865613del , CM000681.2:g.41860544_41865613del GRCh38
NG_007080.3:g.5627_10696del

Transcript Alleles

HGVS Amino-acid change
ENST00000598261.2:c.1-231_186-3418del
ENST00000598742.6:c.1-231_173-3418del
ENST00000600467.6:c.-1+99_173-3418del
ENST00000221975.6:c.-212-241_-50-3418del
ENST00000593863.5:c.-1+50_173-3418del
ENST00000598742.5:c.1-231_173-3418del
ENST00000600467.5:c.-1+99_173-3418del
ENST00000601492.5:c.1-231_254-3418del
NM_001022.3:c.1-231_173-3418del
NM_001321483.1:c.-1+50_173-3418del
NM_001321484.1:c.-1+99_173-3418del
NM_001321485.1:c.1-231_186-3418del
XM_017027113.2:c.1-231_173-3418del
NM_001022.4:c.1-231_173-3418del
NM_001321483.2:c.-1+50_173-3418del
NM_001321484.2:c.-1+99_173-3418del
NM_001321485.2:c.1-231_186-3418del
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