Canonical Allele Identifier: CA2672190084

Gene: IL15

Linked Data

• gnomAD v4: 4-141733038-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733040_141733041del , CM000666.2:g.141733040_141733041del	GRCh38
NC_000004.11:g.142654193_142654194del , CM000666.1:g.142654193_142654194del	GRCh37
NC_000004.10:g.142873643_142873644del	NCBI36
NG_029605.1:g.101445_101446del
NG_029605.2:g.101445_101446del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*192_*193del MANE Select	ENSP00000323505.4:n.*192_*193del
ENST00000296545.11:c.*192_*193del	ENSP00000296545.7:n.*192_*193del
ENST00000320650.8:c.*192_*193del	ENSP00000323505.4:n.*192_*193del
ENST00000394159.2:c.600_601del	ENSP00000377714.1:n.600_601del
ENST00000477265.5:c.*192_*193del	ENSP00000436914.1:n.*192_*193del
ENST00000514653.5:c.*192_*193del	ENSP00000422271.1:n.*192_*193del
ENST00000529613.5:c.*192_*193del	ENSP00000435462.1:n.*192_*193del
NM_000585.4:c.*192_*193del	NP_000576.1:n.*192_*193del
NM_172175.2:c.*192_*193del	NP_751915.1:n.*192_*193del
NR_037840.2:n.1531_1532del
NM_000585.5:c.*192_*193del MANE Select	NP_000576.1:n.*192_*193del
NM_172175.3:c.*192_*193del	NP_751915.1:n.*192_*193del
NR_037840.3:n.1544_1545del