Canonical Allele Identifier: CA5397051

Gene: IL15RA

Linked Data

• ClinVar Variation Id: 1232028
• ClinVar RCV Id: RCV001620114
• dbSNP Id: rs2228059
• ExAC: 10:6002368 T / G
• gnomAD v2: 10-6002368-T-G
• gnomAD v3: 10-5960405-T-G
• gnomAD v4: 10-5960405-T-G
• MyVariant Identifiers: chr10:g.6002368T>G (hg19) ; chr10:g.5960405T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.5960405T>G , CM000672.2:g.5960405T>G	GRCh38
NC_000010.10:g.6002368T>G , CM000672.1:g.6002368T>G	GRCh37
NC_000010.9:g.6042374T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000379977.8:c.545A>C MANE Select	ENSP00000369312.3:p.Asn182Thr
ENST00000379971.5:c.251A>C	ENSP00000369306.1:p.Asn84Thr
ENST00000379972.6:n.670A>C
ENST00000379974.1:n.566A>C
ENST00000379977.7:c.545A>C	ENSP00000369312.3:p.Asn182Thr
ENST00000397246.7:c.338A>C	ENSP00000380420.4:p.Asn113Thr
ENST00000397248.6:c.803A>C	ENSP00000380421.3:p.Asn268Thr
ENST00000397250.6:c.251A>C	ENSP00000380422.2:p.Asn84Thr
ENST00000397251.7:c.698A>C	ENSP00000380423.3:p.Asn233Thr
ENST00000397255.7:c.545A>C	ENSP00000380426.3:p.Asn182Thr
ENST00000429135.2:c.446A>C	ENSP00000395113.2:p.Asn149Thr
ENST00000435171.6:c.163A>C
ENST00000447291.5:c.253A>C
ENST00000453922.1:c.434A>C	ENSP00000405107.1:p.Asn145Thr
ENST00000525219.6:c.437A>C	ENSP00000431529.2:p.Asn146Thr
ENST00000528354.5:c.446A>C	ENSP00000435454.1:p.Asn149Thr
ENST00000530685.5:c.446A>C	ENSP00000435995.1:p.Asn149Thr
ENST00000532039.5:c.259A>C
ENST00000532948.5:n.620A>C
ENST00000534292.5:n.726A>C
ENST00000618528.4:c.698A>C	ENSP00000479938.1:p.Asn233Thr
ENST00000620345.4:c.698A>C	ENSP00000479839.1:p.Asn233Thr
ENST00000620865.4:c.698A>C	ENSP00000478525.1:p.Asn233Thr
ENST00000622442.4:c.698A>C	ENSP00000480949.1:p.Asn233Thr
NM_001243539.1:c.437A>C	NP_001230468.1:p.Asn146Thr
NM_001256765.1:c.803A>C	NP_001243694.1:p.Asn268Thr
NM_002189.3:c.545A>C	NP_002180.1:p.Asn182Thr
NM_172200.2:c.446A>C	NP_751950.2:p.Asn149Thr
NR_046362.1:n.574A>C
XM_011519461.1:c.872A>C	XP_011517763.1:p.Asn291Thr
XM_011519462.1:c.803A>C	XP_011517764.1:p.Asn268Thr
XM_011519463.1:c.773A>C	XP_011517765.1:p.Asn258Thr
XM_011519464.1:c.719A>C	XP_011517766.1:p.Asn240Thr
XM_011519465.1:c.872A>C	XP_011517767.1:p.Asn291Thr
XM_011519466.1:c.872A>C	XP_011517768.1:p.Asn291Thr
XM_011519467.1:c.650A>C	XP_011517769.1:p.Asn217Thr
XM_011519468.1:c.872A>C	XP_011517770.1:p.Asn291Thr
XM_011519469.1:c.773A>C	XP_011517771.1:p.Asn258Thr
XM_011519470.1:c.551A>C	XP_011517772.1:p.Asn184Thr
XM_011519471.1:c.524A>C	XP_011517773.1:p.Asn175Thr
XM_011519472.1:c.455A>C	XP_011517774.1:p.Asn152Thr
XM_011519473.1:c.437A>C	XP_011517775.1:p.Asn146Thr
XM_011519474.1:c.425A>C	XP_011517776.1:p.Asn142Thr
XM_011519475.1:c.356A>C	XP_011517777.1:p.Asn119Thr
XM_011519476.1:c.356A>C	XP_011517778.1:p.Asn119Thr
XM_011519477.1:c.356A>C	XP_011517779.1:p.Asn119Thr
NM_001351095.1:c.620A>C	NP_001338024.1:p.Asn207Thr
NM_001351096.1:c.437A>C	NP_001338025.1:p.Asn146Thr
NM_001351097.1:c.338A>C	NP_001338026.1:p.Asn113Thr
XM_011519461.2:c.872A>C	XP_011517763.1:p.Asn291Thr
XM_011519462.2:c.803A>C	XP_011517764.1:p.Asn268Thr
XM_011519463.2:c.773A>C	XP_011517765.1:p.Asn258Thr
XM_011519464.2:c.719A>C	XP_011517766.1:p.Asn240Thr
XM_011519466.2:c.872A>C	XP_011517768.1:p.Asn291Thr
XM_011519467.2:c.650A>C	XP_011517769.1:p.Asn217Thr
XM_011519470.2:c.551A>C	XP_011517772.1:p.Asn184Thr
XM_011519471.2:c.524A>C	XP_011517773.1:p.Asn175Thr
XM_011519472.2:c.455A>C	XP_011517774.1:p.Asn152Thr
XM_011519474.2:c.425A>C	XP_011517776.1:p.Asn142Thr
XM_011519475.2:c.356A>C	XP_011517777.1:p.Asn119Thr
XM_011519476.2:c.356A>C	XP_011517778.1:p.Asn119Thr
XM_011519477.2:c.356A>C	XP_011517779.1:p.Asn119Thr
XM_017016195.1:c.719A>C	XP_016871684.1:p.Asn240Thr
XM_017016196.1:c.437A>C	XP_016871685.1:p.Asn146Thr
XM_017016197.2:c.437A>C	XP_016871686.1:p.Asn146Thr
XM_017016198.1:c.524A>C	XP_016871687.1:p.Asn175Thr
XM_017016200.2:c.338A>C	XP_016871689.1:p.Asn113Thr
XM_024447983.1:c.437A>C	XP_024303751.1:p.Asn146Thr
XR_001747348.1:n.613T>G
NM_002189.4:c.545A>C MANE Select	NP_002180.1:p.Asn182Thr
NM_001351097.2:c.338A>C	NP_001338026.1:p.Asn113Thr
NM_172200.3:c.446A>C	NP_751950.2:p.Asn149Thr
NR_046362.2:n.433A>C
NM_001243539.2:c.437A>C	NP_001230468.1:p.Asn146Thr
NM_001351095.2:c.620A>C	NP_001338024.1:p.Asn207Thr