Canonical Allele Identifier: CA358388180

Gene: IL15

Linked Data

• MyVariant Identifiers: chr4:g.142653997C>G (hg19) ; chr4:g.141732844C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141732844C>G , CM000666.2:g.141732844C>G	GRCh38
NC_000004.11:g.142653997C>G , CM000666.1:g.142653997C>G	GRCh37
NC_000004.10:g.142873447C>G	NCBI36
NG_029605.1:g.101249C>G
NG_029605.2:g.101249C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000320650.9:c.485C>G MANE Select	ENSP00000323505.4:p.Ser162Cys
ENST00000296545.11:c.485C>G	ENSP00000296545.7:p.Ser162Cys
ENST00000320650.8:c.485C>G	ENSP00000323505.4:p.Ser162Cys
ENST00000394159.2:c.404C>G	ENSP00000377714.1:p.Ser135Cys
ENST00000477265.5:c.404C>G	ENSP00000436914.1:p.Ser135Cys
ENST00000514653.5:c.404C>G	ENSP00000422271.1:p.Ser135Cys
ENST00000529613.5:c.485C>G	ENSP00000435462.1:p.Ser162Cys
NM_000585.4:c.485C>G	NP_000576.1:p.Ser162Cys
NM_172175.2:c.404C>G	NP_751915.1:p.Ser135Cys
NR_037840.2:n.1335C>G
NM_000585.5:c.485C>G MANE Select	NP_000576.1:p.Ser162Cys
NM_172175.3:c.404C>G	NP_751915.1:p.Ser135Cys
NR_037840.3:n.1348C>G