Canonical Allele Identifier: CA788196470
Gene: IL15 HGNC NCBI

Linked Data

dbSNP Id: rs1407335714
gnomAD v4: 4-141733126-TA-T
MyVariant Identifiers: chr4:g.142654280del (hg19) chr4:g.141733127del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733131del , CM000666.2:g.141733131del GRCh38
NC_000004.11:g.142654284del , CM000666.1:g.142654284del GRCh37
NC_000004.10:g.142873734del NCBI36
NG_029605.1:g.101536del
NG_029605.2:g.101536del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*283del MANE Select ENSP00000323505.4:n.*283del
ENST00000296545.11:c.*283del ENSP00000296545.7:n.*283del
ENST00000320650.8:c.*283del ENSP00000323505.4:n.*283del
ENST00000394159.2:c.691del ENSP00000377714.1:n.691del
ENST00000477265.5:c.*283del ENSP00000436914.1:n.*283del
ENST00000514653.5:c.*283del ENSP00000422271.1:n.*283del
NM_000585.4:c.*283del NP_000576.1:n.*283del
NM_172175.2:c.*283del NP_751915.1:n.*283del
NR_037840.2:n.1622del
NM_000585.5:c.*283del MANE Select NP_000576.1:n.*283del
NM_172175.3:c.*283del NP_751915.1:n.*283del
NR_037840.3:n.1635del
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