Canonical Allele Identifier: CA1499394540

Gene: IL15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733141_141733144delinsGTGT , CM000666.2:g.141733141_141733144delinsGTGT	GRCh38
NC_000004.11:g.142654294_142654297delinsGTGT , CM000666.1:g.142654294_142654297delinsGTGT	GRCh37
NC_000004.10:g.142873744_142873747delinsGTGT	NCBI36
NG_029605.1:g.101546_101549delinsGTGT
NG_029605.2:g.101546_101549delinsGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*293_*296delinsGTGT MANE Select	ENSP00000323505.4:n.*293_*296delinsGTGT
ENST00000296545.11:c.*293_*296delinsGTGT	ENSP00000296545.7:n.*293_*296delinsGTGT
ENST00000320650.8:c.*293_*296delinsGTGT	ENSP00000323505.4:n.*293_*296delinsGTGT
ENST00000394159.2:c.701_704delinsGTGT	ENSP00000377714.1:n.701_704delinsGTGT
ENST00000477265.5:c.*293_*296delinsGTGT	ENSP00000436914.1:n.*293_*296delinsGTGT
ENST00000514653.5:c.*293_*296delinsGTGT	ENSP00000422271.1:n.*293_*296delinsGTGT
NM_000585.4:c.*293_*296delinsGTGT	NP_000576.1:n.*293_*296delinsGTGT
NM_172175.2:c.*293_*296delinsGTGT	NP_751915.1:n.*293_*296delinsGTGT
NR_037840.2:n.1632_1635delinsGTGT
NM_000585.5:c.*293_*296delinsGTGT MANE Select	NP_000576.1:n.*293_*296delinsGTGT
NM_172175.3:c.*293_*296delinsGTGT	NP_751915.1:n.*293_*296delinsGTGT
NR_037840.3:n.1645_1648delinsGTGT