Canonical Allele Identifier: CA1068842365
Gene: IL15 HGNC NCBI

Linked Data

dbSNP Id: rs1730515221

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733337_141733338del , CM000666.2:g.141733337_141733338del GRCh38
NC_000004.11:g.142654490_142654491del , CM000666.1:g.142654490_142654491del GRCh37
NC_000004.10:g.142873940_142873941del NCBI36
NG_029605.1:g.101742_101743del
NG_029605.2:g.101742_101743del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*489_*490del MANE Select ENSP00000323505.4:n.*489_*490del
ENST00000296545.11:c.*489_*490del ENSP00000296545.7:n.*489_*490del
ENST00000320650.8:c.*489_*490del ENSP00000323505.4:n.*489_*490del
ENST00000394159.2:c.897_898del ENSP00000377714.1:n.897_898del
ENST00000477265.5:c.*489_*490del ENSP00000436914.1:n.*489_*490del
NM_000585.4:c.*489_*490del NP_000576.1:n.*489_*490del
NM_172175.2:c.*489_*490del NP_751915.1:n.*489_*490del
NR_037840.2:n.1828_1829del
NM_000585.5:c.*489_*490del MANE Select NP_000576.1:n.*489_*490del
NM_172175.3:c.*489_*490del NP_751915.1:n.*489_*490del
NR_037840.3:n.1841_1842del