Canonical Allele Identifier: CA2581443892
Gene: IL15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733394T>G , CM000666.2:g.141733394T>G GRCh38
NC_000004.11:g.142654547T>G , CM000666.1:g.142654547T>G GRCh37
NC_000004.10:g.142873997T>G NCBI36
NG_029605.1:g.101799T>G
NG_029605.2:g.101799T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320650.9:c.*546T>G MANE Select ENSP00000323505.4:n.*546T>G
ENST00000296545.11:c.*546T>G ENSP00000296545.7:n.*546T>G
ENST00000320650.8:c.*546T>G ENSP00000323505.4:n.*546T>G
ENST00000394159.2:c.954T>G ENSP00000377714.1:n.954T>G
ENST00000477265.5:c.*546T>G ENSP00000436914.1:n.*546T>G
NM_000585.4:c.*546T>G NP_000576.1:n.*546T>G
NM_172175.2:c.*546T>G NP_751915.1:n.*546T>G
NR_037840.2:n.1885T>G
NM_000585.5:c.*546T>G MANE Select NP_000576.1:n.*546T>G
NM_172175.3:c.*546T>G NP_751915.1:n.*546T>G
NR_037840.3:n.1898T>G
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