Canonical Allele Identifier: CA2707546867
Gene: IL15 HGNC NCBI

Linked Data

dbSNP Id: rs2152195102

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733137dup , CM000666.2:g.141733137dup GRCh38
NC_000004.11:g.142654290dup , CM000666.1:g.142654290dup GRCh37
NC_000004.10:g.142873740dup NCBI36
NG_029605.1:g.101542dup
NG_029605.2:g.101542dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*289dup MANE Select ENSP00000323505.4:n.*289dup
ENST00000296545.11:c.*289dup ENSP00000296545.7:n.*289dup
ENST00000320650.8:c.*289dup ENSP00000323505.4:n.*289dup
ENST00000394159.2:c.697dup ENSP00000377714.1:n.697dup
ENST00000477265.5:c.*289dup ENSP00000436914.1:n.*289dup
ENST00000514653.5:c.*289dup ENSP00000422271.1:n.*289dup
NM_000585.4:c.*289dup NP_000576.1:n.*289dup
NM_172175.2:c.*289dup NP_751915.1:n.*289dup
NR_037840.2:n.1628dup
NM_000585.5:c.*289dup MANE Select NP_000576.1:n.*289dup
NM_172175.3:c.*289dup NP_751915.1:n.*289dup
NR_037840.3:n.1641dup