Canonical Allele Identifier: CA2672190078

Gene: IL15

Linked Data

• gnomAD v4: 4-141733034-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733034_141733035insC , CM000666.2:g.141733034_141733035insC	GRCh38
NC_000004.11:g.142654187_142654188insC , CM000666.1:g.142654187_142654188insC	GRCh37
NC_000004.10:g.142873637_142873638insC	NCBI36
NG_029605.1:g.101439_101440insC
NG_029605.2:g.101439_101440insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*186_*187insC MANE Select	ENSP00000323505.4:n.*186_*187insC
ENST00000296545.11:c.*186_*187insC	ENSP00000296545.7:n.*186_*187insC
ENST00000320650.8:c.*186_*187insC	ENSP00000323505.4:n.*186_*187insC
ENST00000394159.2:c.594_595insC	ENSP00000377714.1:n.594_595insC
ENST00000477265.5:c.*186_*187insC	ENSP00000436914.1:n.*186_*187insC
ENST00000514653.5:c.*186_*187insC	ENSP00000422271.1:n.*186_*187insC
ENST00000529613.5:c.*186_*187insC	ENSP00000435462.1:n.*186_*187insC
NM_000585.4:c.*186_*187insC	NP_000576.1:n.*186_*187insC
NM_172175.2:c.*186_*187insC	NP_751915.1:n.*186_*187insC
NR_037840.2:n.1525_1526insC
NM_000585.5:c.*186_*187insC MANE Select	NP_000576.1:n.*186_*187insC
NM_172175.3:c.*186_*187insC	NP_751915.1:n.*186_*187insC
NR_037840.3:n.1538_1539insC