Canonical Allele Identifier: CA1499394833
Gene: IL15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733486G= , CM000666.2:g.141733486G= GRCh38
NC_000004.11:g.142654639G= , CM000666.1:g.142654639G= GRCh37
NC_000004.10:g.142874089G= NCBI36
NG_029605.1:g.101891G=
NG_029605.2:g.101891G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*638G= MANE Select ENSP00000323505.4:n.*638G=
ENST00000296545.11:c.*638G= ENSP00000296545.7:n.*638G=
ENST00000394159.2:c.1046G= ENSP00000377714.1:n.1046G=
NM_000585.4:c.*638G= NP_000576.1:n.*638G=
NM_172175.2:c.*638G= NP_751915.1:n.*638G=
NR_037840.2:n.1977G=
NM_000585.5:c.*638G= MANE Select NP_000576.1:n.*638G=
NM_172175.3:c.*638G= NP_751915.1:n.*638G=
NR_037840.3:n.1990G=
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