Canonical Allele Identifier: CA2672190227
Gene: IL15 HGNC NCBI

Linked Data

gnomAD v4: 4-141733263-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733263C>A , CM000666.2:g.141733263C>A GRCh38
NC_000004.11:g.142654416C>A , CM000666.1:g.142654416C>A GRCh37
NC_000004.10:g.142873866C>A NCBI36
NG_029605.1:g.101668C>A
NG_029605.2:g.101668C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*415C>A MANE Select ENSP00000323505.4:n.*415C>A
ENST00000296545.11:c.*415C>A ENSP00000296545.7:n.*415C>A
ENST00000320650.8:c.*415C>A ENSP00000323505.4:n.*415C>A
ENST00000394159.2:c.823C>A ENSP00000377714.1:n.823C>A
ENST00000477265.5:c.*415C>A ENSP00000436914.1:n.*415C>A
NM_000585.4:c.*415C>A NP_000576.1:n.*415C>A
NM_172175.2:c.*415C>A NP_751915.1:n.*415C>A
NR_037840.2:n.1754C>A
NM_000585.5:c.*415C>A MANE Select NP_000576.1:n.*415C>A
NM_172175.3:c.*415C>A NP_751915.1:n.*415C>A
NR_037840.3:n.1767C>A
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