Canonical Allele Identifier: CA1499394767
Gene: IL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733413A= , CM000666.2:g.141733413A= GRCh38
NC_000004.11:g.142654566A= , CM000666.1:g.142654566A= GRCh37
NC_000004.10:g.142874016A= NCBI36
NG_029605.1:g.101818A=
NG_029605.2:g.101818A=

Transcript Alleles

HGVS Amino-acid change
ENST00000320650.9:c.*565A= MANE Select ENSP00000323505.4:n.*565A=
ENST00000296545.11:c.*565A= ENSP00000296545.7:n.*565A=
ENST00000320650.8:c.*565A= ENSP00000323505.4:n.*565A=
ENST00000394159.2:c.973A= ENSP00000377714.1:n.973A=
ENST00000477265.5:c.*565A= ENSP00000436914.1:n.*565A=
NM_000585.4:c.*565A= NP_000576.1:n.*565A=
NM_172175.2:c.*565A= NP_751915.1:n.*565A=
NR_037840.2:n.1904A=
NM_000585.5:c.*565A= MANE Select NP_000576.1:n.*565A=
NM_172175.3:c.*565A= NP_751915.1:n.*565A=
NR_037840.3:n.1917A=