Canonical Allele Identifier: CA358388153

Gene: IL15

Linked Data

• MyVariant Identifiers: chr4:g.142653985T>C (hg19) ; chr4:g.141732832T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141732832T>C , CM000666.2:g.141732832T>C	GRCh38
NC_000004.11:g.142653985T>C , CM000666.1:g.142653985T>C	GRCh37
NC_000004.10:g.142873435T>C	NCBI36
NG_029605.1:g.101237T>C
NG_029605.2:g.101237T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000320650.9:c.473T>C MANE Select	ENSP00000323505.4:p.Phe158Ser
ENST00000296545.11:c.473T>C	ENSP00000296545.7:p.Phe158Ser
ENST00000320650.8:c.473T>C	ENSP00000323505.4:p.Phe158Ser
ENST00000394159.2:c.392T>C	ENSP00000377714.1:p.Phe131Ser
ENST00000477265.5:c.392T>C	ENSP00000436914.1:p.Phe131Ser
ENST00000514653.5:c.392T>C	ENSP00000422271.1:p.Phe131Ser
ENST00000529613.5:c.473T>C	ENSP00000435462.1:p.Phe158Ser
NM_000585.4:c.473T>C	NP_000576.1:p.Phe158Ser
NM_172175.2:c.392T>C	NP_751915.1:p.Phe131Ser
NR_037840.2:n.1323T>C
NM_000585.5:c.473T>C MANE Select	NP_000576.1:p.Phe158Ser
NM_172175.3:c.392T>C	NP_751915.1:p.Phe131Ser
NR_037840.3:n.1336T>C