Canonical Allele Identifier: CA1499366910
Community Standard Title: NM_000585.5(IL15):c.-221-6867G=
Gene: IL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141649319G= , CM000666.2:g.141649319G= GRCh38
NC_000004.11:g.142570472G= , CM000666.1:g.142570472G= GRCh37
NC_000004.10:g.142789922G= NCBI36
NG_029605.1:g.17724G=
NG_029605.2:g.17724G=

Transcript Alleles

HGVS Amino-acid Change
NM_000585.5:c.-221-6867G= MANE Select NP_000576.1:n.-221-6867G=
ENST00000320650.9:c.-221-6867G= MANE Select ENSP00000323505.4:n.-221-6867G=
NM_000585.4:c.-221-6867G= NP_000576.1:n.-221-6867G=
NM_172175.2:c.-623-6867G= NP_751915.1:n.-623-6867G=
NM_172175.3:c.-623-6867G= NP_751915.1:n.-623-6867G=
NR_037840.2:n.630-6867G=
NR_037840.3:n.643-6867G=
ENST00000296545.11:c.-221-6867G= ENSP00000296545.7:n.-221-6867G=
ENST00000320650.8:c.-221-6867G= ENSP00000323505.4:n.-221-6867G=
ENST00000514653.5:c.-623-6867G= ENSP00000422271.1:n.-623-6867G=
ENST00000529613.5:c.-314+12095G= ENSP00000435462.1:n.-314+12095G=