Canonical Allele Identifier: CA1499394691

Gene: IL15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733326A= , CM000666.2:g.141733326A=	GRCh38
NC_000004.11:g.142654479A= , CM000666.1:g.142654479A=	GRCh37
NC_000004.10:g.142873929A=	NCBI36
NG_029605.1:g.101731A=
NG_029605.2:g.101731A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*478A= MANE Select	ENSP00000323505.4:n.*478A=
ENST00000296545.11:c.*478A=	ENSP00000296545.7:n.*478A=
ENST00000320650.8:c.*478A=	ENSP00000323505.4:n.*478A=
ENST00000394159.2:c.886A=	ENSP00000377714.1:n.886A=
ENST00000477265.5:c.*478A=	ENSP00000436914.1:n.*478A=
NM_000585.4:c.*478A=	NP_000576.1:n.*478A=
NM_172175.2:c.*478A=	NP_751915.1:n.*478A=
NR_037840.2:n.1817A=
NM_000585.5:c.*478A= MANE Select	NP_000576.1:n.*478A=
NM_172175.3:c.*478A=	NP_751915.1:n.*478A=
NR_037840.3:n.1830A=