Canonical Allele Identifier: CA2672190080

Gene: IL15

Linked Data

• gnomAD v4: 4-141733034-GTGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733035_141733037del , CM000666.2:g.141733035_141733037del	GRCh38
NC_000004.11:g.142654188_142654190del , CM000666.1:g.142654188_142654190del	GRCh37
NC_000004.10:g.142873638_142873640del	NCBI36
NG_029605.1:g.101440_101442del
NG_029605.2:g.101440_101442del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*187_*189del MANE Select	ENSP00000323505.4:n.*187_*189del
ENST00000296545.11:c.*187_*189del	ENSP00000296545.7:n.*187_*189del
ENST00000320650.8:c.*187_*189del	ENSP00000323505.4:n.*187_*189del
ENST00000394159.2:c.595_597del	ENSP00000377714.1:n.595_597del
ENST00000477265.5:c.*187_*189del	ENSP00000436914.1:n.*187_*189del
ENST00000514653.5:c.*187_*189del	ENSP00000422271.1:n.*187_*189del
ENST00000529613.5:c.*187_*189del	ENSP00000435462.1:n.*187_*189del
NM_000585.4:c.*187_*189del	NP_000576.1:n.*187_*189del
NM_172175.2:c.*187_*189del	NP_751915.1:n.*187_*189del
NR_037840.2:n.1526_1528del
NM_000585.5:c.*187_*189del MANE Select	NP_000576.1:n.*187_*189del
NM_172175.3:c.*187_*189del	NP_751915.1:n.*187_*189del
NR_037840.3:n.1539_1541del