Canonical Allele Identifier: CA1499382145
Community Standard Title: NM_000585.5(IL15):c.12+8A=
Gene: IL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141719484A= , CM000666.2:g.141719484A= GRCh38
NC_000004.11:g.142640637A= , CM000666.1:g.142640637A= GRCh37
NC_000004.10:g.142860087A= NCBI36
NG_029605.1:g.87889A=
NG_029605.2:g.87889A=

Transcript Alleles

HGVS Amino-acid Change
NM_000585.5:c.12+8A= MANE Select NP_000576.1:n.12+8A=
ENST00000320650.9:c.12+8A= MANE Select ENSP00000323505.4:n.12+8A=
NM_000585.4:c.12+8A= NP_000576.1:n.12+8A=
NM_172175.2:c.-189+8A= NP_751915.1:n.-189+8A=
NM_172175.3:c.-189+8A= NP_751915.1:n.-189+8A=
NR_037840.2:n.862+8A=
NR_037840.3:n.875+8A=
ENST00000296545.11:c.12+8A= ENSP00000296545.7:n.12+8A=
ENST00000320650.8:c.12+8A= ENSP00000323505.4:n.12+8A=
ENST00000477265.5:c.-189+8A= ENSP00000436914.1:n.-189+8A=
ENST00000505351.1:n.346+8A=
ENST00000514653.5:c.-189+8A= ENSP00000422271.1:n.-189+8A=
ENST00000529613.5:c.12+8A= ENSP00000435462.1:n.12+8A=