Canonical Allele Identifier: CA2672190201
Gene: IL15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733241_141733245del , CM000666.2:g.141733241_141733245del GRCh38
NC_000004.11:g.142654394_142654398del , CM000666.1:g.142654394_142654398del GRCh37
NC_000004.10:g.142873844_142873848del NCBI36
NG_029605.1:g.101646_101650del
NG_029605.2:g.101646_101650del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*393_*397del MANE Select ENSP00000323505.4:n.*393_*397del
ENST00000296545.11:c.*393_*397del ENSP00000296545.7:n.*393_*397del
ENST00000320650.8:c.*393_*397del ENSP00000323505.4:n.*393_*397del
ENST00000394159.2:c.801_805del ENSP00000377714.1:n.801_805del
ENST00000477265.5:c.*393_*397del ENSP00000436914.1:n.*393_*397del
NM_000585.4:c.*393_*397del NP_000576.1:n.*393_*397del
NM_172175.2:c.*393_*397del NP_751915.1:n.*393_*397del
NR_037840.2:n.1732_1736del
NM_000585.5:c.*393_*397del MANE Select NP_000576.1:n.*393_*397del
NM_172175.3:c.*393_*397del NP_751915.1:n.*393_*397del
NR_037840.3:n.1745_1749del