Canonical Allele Identifier: CA1499394814
Gene: IL15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733459A= , CM000666.2:g.141733459A= GRCh38
NC_000004.11:g.142654612A= , CM000666.1:g.142654612A= GRCh37
NC_000004.10:g.142874062A= NCBI36
NG_029605.1:g.101864A=
NG_029605.2:g.101864A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*611A= MANE Select ENSP00000323505.4:n.*611A=
ENST00000296545.11:c.*611A= ENSP00000296545.7:n.*611A=
ENST00000394159.2:c.1019A= ENSP00000377714.1:n.1019A=
NM_000585.4:c.*611A= NP_000576.1:n.*611A=
NM_172175.2:c.*611A= NP_751915.1:n.*611A=
NR_037840.2:n.1950A=
NM_000585.5:c.*611A= MANE Select NP_000576.1:n.*611A=
NM_172175.3:c.*611A= NP_751915.1:n.*611A=
NR_037840.3:n.1963A=
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