Canonical Allele Identifier: CA1499380582
Community Standard Title: NM_000585.5(IL15):c.-99-1768T=
Gene: IL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141717598T= , CM000666.2:g.141717598T= GRCh38
NC_000004.11:g.142638751T= , CM000666.1:g.142638751T= GRCh37
NC_000004.10:g.142858201T= NCBI36
NG_029605.1:g.86003T=
NG_029605.2:g.86003T=

Transcript Alleles

HGVS Amino-acid Change
NM_000585.5:c.-99-1768T= MANE Select NP_000576.1:n.-99-1768T=
ENST00000320650.9:c.-99-1768T= MANE Select ENSP00000323505.4:n.-99-1768T=
NM_000585.4:c.-99-1768T= NP_000576.1:n.-99-1768T=
NM_172175.2:c.-287-1780T= NP_751915.1:n.-287-1780T=
NM_172175.3:c.-287-1780T= NP_751915.1:n.-287-1780T=
NR_037840.2:n.752-1768T=
NR_037840.3:n.765-1768T=
ENST00000296545.11:c.-99-1768T= ENSP00000296545.7:n.-99-1768T=
ENST00000320650.8:c.-99-1768T= ENSP00000323505.4:n.-99-1768T=
ENST00000477265.5:c.-2067T= ENSP00000436914.1:n.-2067T=
ENST00000514653.5:c.-287-1780T= ENSP00000422271.1:n.-287-1780T=
ENST00000529613.5:c.-99-1768T= ENSP00000435462.1:n.-99-1768T=