Canonical Allele Identifier: CA358386145

Gene: IL15

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141717598T>C , CM000666.2:g.141717598T>C	GRCh38
NC_000004.11:g.142638751T>C , CM000666.1:g.142638751T>C	GRCh37
NC_000004.10:g.142858201T>C	NCBI36
NG_029605.1:g.86003T>C
NG_029605.2:g.86003T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.-99-1768T>C MANE Select	ENSP00000323505.4:n.-99-1768T>C
ENST00000296545.11:c.-99-1768T>C	ENSP00000296545.7:n.-99-1768T>C
ENST00000320650.8:c.-99-1768T>C	ENSP00000323505.4:n.-99-1768T>C
ENST00000477265.5:c.-2067T>C	ENSP00000436914.1:n.-2067T>C
ENST00000514653.5:c.-287-1780T>C	ENSP00000422271.1:n.-287-1780T>C
ENST00000529613.5:c.-99-1768T>C	ENSP00000435462.1:n.-99-1768T>C
NM_000585.4:c.-99-1768T>C	NP_000576.1:n.-99-1768T>C
NM_172175.2:c.-287-1780T>C	NP_751915.1:n.-287-1780T>C
NR_037840.2:n.752-1768T>C
NM_000585.5:c.-99-1768T>C MANE Select	NP_000576.1:n.-99-1768T>C
NM_172175.3:c.-287-1780T>C	NP_751915.1:n.-287-1780T>C
NR_037840.3:n.765-1768T>C