Canonical Allele Identifier: CA358388171

Gene: IL15

Linked Data

• MyVariant Identifiers: chr4:g.142653993A>T (hg19) ; chr4:g.141732840A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141732840A>T , CM000666.2:g.141732840A>T	GRCh38
NC_000004.11:g.142653993A>T , CM000666.1:g.142653993A>T	GRCh37
NC_000004.10:g.142873443A>T	NCBI36
NG_029605.1:g.101245A>T
NG_029605.2:g.101245A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000320650.9:c.481A>T MANE Select	ENSP00000323505.4:p.Thr161Ser
ENST00000296545.11:c.481A>T	ENSP00000296545.7:p.Thr161Ser
ENST00000320650.8:c.481A>T	ENSP00000323505.4:p.Thr161Ser
ENST00000394159.2:c.400A>T	ENSP00000377714.1:p.Thr134Ser
ENST00000477265.5:c.400A>T	ENSP00000436914.1:p.Thr134Ser
ENST00000514653.5:c.400A>T	ENSP00000422271.1:p.Thr134Ser
ENST00000529613.5:c.481A>T	ENSP00000435462.1:p.Thr161Ser
NM_000585.4:c.481A>T	NP_000576.1:p.Thr161Ser
NM_172175.2:c.400A>T	NP_751915.1:p.Thr134Ser
NR_037840.2:n.1331A>T
NM_000585.5:c.481A>T MANE Select	NP_000576.1:p.Thr161Ser
NM_172175.3:c.400A>T	NP_751915.1:p.Thr134Ser
NR_037840.3:n.1344A>T