Canonical Allele Identifier: CA788196451

Gene: IL15

Linked Data

• dbSNP Id: rs1263639770
• gnomAD v4: 4-141733072-TTTTAA-T
• MyVariant Identifiers: chr4:g.142654226_142654230del (hg19) ; chr4:g.141733073_141733077del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733077_141733081del , CM000666.2:g.141733077_141733081del	GRCh38
NC_000004.11:g.142654230_142654234del , CM000666.1:g.142654230_142654234del	GRCh37
NC_000004.10:g.142873680_142873684del	NCBI36
NG_029605.1:g.101482_101486del
NG_029605.2:g.101482_101486del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*229_*233del MANE Select	ENSP00000323505.4:n.*229_*233del
ENST00000296545.11:c.*229_*233del	ENSP00000296545.7:n.*229_*233del
ENST00000320650.8:c.*229_*233del	ENSP00000323505.4:n.*229_*233del
ENST00000394159.2:c.637_641del	ENSP00000377714.1:n.637_641del
ENST00000477265.5:c.*229_*233del	ENSP00000436914.1:n.*229_*233del
ENST00000514653.5:c.*229_*233del	ENSP00000422271.1:n.*229_*233del
ENST00000529613.5:c.*229_*233del	ENSP00000435462.1:n.*229_*233del
NM_000585.4:c.*229_*233del	NP_000576.1:n.*229_*233del
NM_172175.2:c.*229_*233del	NP_751915.1:n.*229_*233del
NR_037840.2:n.1568_1572del
NM_000585.5:c.*229_*233del MANE Select	NP_000576.1:n.*229_*233del
NM_172175.3:c.*229_*233del	NP_751915.1:n.*229_*233del
NR_037840.3:n.1581_1585del