Canonical Allele Identifier: CA441598720

Gene: IL15

Linked Data

• dbSNP Id: rs1196586416
• gnomAD v2: 4-142654221-A-AT
• gnomAD v3: 4-141733068-A-AT
• gnomAD v4: 4-141733068-A-AT
• MyVariant Identifiers: chr4:g.142654222_142654223insT (hg19) ; chr4:g.142654221_142654222insT (hg19) ; chr4:g.141733069_141733070insT (hg38) ; chr4:g.141733068_141733069insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733075dup , CM000666.2:g.141733075dup	GRCh38
NC_000004.11:g.142654228dup , CM000666.1:g.142654228dup	GRCh37
NC_000004.10:g.142873678dup	NCBI36
NG_029605.1:g.101480dup
NG_029605.2:g.101480dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*227dup MANE Select	ENSP00000323505.4:n.*227dup
ENST00000296545.11:c.*227dup	ENSP00000296545.7:n.*227dup
ENST00000320650.8:c.*227dup	ENSP00000323505.4:n.*227dup
ENST00000394159.2:c.635dup	ENSP00000377714.1:n.635dup
ENST00000477265.5:c.*227dup	ENSP00000436914.1:n.*227dup
ENST00000514653.5:c.*227dup	ENSP00000422271.1:n.*227dup
ENST00000529613.5:c.*227dup	ENSP00000435462.1:n.*227dup
NM_000585.4:c.*227dup	NP_000576.1:n.*227dup
NM_172175.2:c.*227dup	NP_751915.1:n.*227dup
NR_037840.2:n.1566dup
NM_000585.5:c.*227dup MANE Select	NP_000576.1:n.*227dup
NM_172175.3:c.*227dup	NP_751915.1:n.*227dup
NR_037840.3:n.1579dup