Canonical Allele Identifier: CA1887999416
Community Standard Title: NM_002189.4(IL15RA):c.545A= (p.Asn182=)
Gene: IL15RA HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_002189.4:c.545A= MANE Select NP_002180.1:p.Asn182=
ENST00000379977.8:c.545A= MANE Select ENSP00000369312.3:p.Asn182=
NM_001243539.1:c.437A= NP_001230468.1:p.Asn146=
NM_001243539.2:c.437A= NP_001230468.1:p.Asn146=
NM_001256765.1:c.803A= NP_001243694.1:p.Asn268=
NM_001351095.1:c.620A= NP_001338024.1:p.Asn207=
NM_001351095.2:c.620A= NP_001338024.1:p.Asn207=
NM_001351096.1:c.437A= NP_001338025.1:p.Asn146=
NM_001351097.1:c.338A= NP_001338026.1:p.Asn113=
NM_001351097.2:c.338A= NP_001338026.1:p.Asn113=
NM_002189.3:c.545A= NP_002180.1:p.Asn182=
NM_172200.2:c.446A= NP_751950.2:p.Asn149=
NM_172200.3:c.446A= NP_751950.2:p.Asn149=
NR_046362.1:n.574A=
NR_046362.2:n.433A=
ENST00000379971.5:c.251A= ENSP00000369306.1:p.Asn84=
ENST00000379972.6:n.670A=
ENST00000379974.1:n.566A=
ENST00000379977.7:c.545A= ENSP00000369312.3:p.Asn182=
ENST00000397246.7:c.338A= ENSP00000380420.4:p.Asn113=
ENST00000397248.6:c.803A= ENSP00000380421.3:p.Asn268=
ENST00000397250.6:c.251A= ENSP00000380422.2:p.Asn84=
ENST00000397251.7:c.698A= ENSP00000380423.3:p.Asn233=
ENST00000397255.7:c.545A= ENSP00000380426.3:p.Asn182=
ENST00000429135.2:c.446A= ENSP00000395113.2:p.Asn149=
ENST00000435171.6:c.163A=
ENST00000447291.5:c.253A=
ENST00000453922.1:c.434A= ENSP00000405107.1:p.Asn145=
ENST00000525219.6:c.437A= ENSP00000431529.2:p.Asn146=
ENST00000528354.5:c.446A= ENSP00000435454.1:p.Asn149=
ENST00000530685.5:c.446A= ENSP00000435995.1:p.Asn149=
ENST00000532039.5:c.259A=
ENST00000532948.5:n.620A=
ENST00000534292.5:n.726A=
ENST00000618528.4:c.698A= ENSP00000479938.1:p.Asn233=
ENST00000620345.4:c.698A= ENSP00000479839.1:p.Asn233=
ENST00000620865.4:c.698A= ENSP00000478525.1:p.Asn233=
ENST00000622442.4:c.698A= ENSP00000480949.1:p.Asn233=
XM_011519461.1:c.872A= XP_011517763.1:p.Asn291=
XM_011519461.2:c.872A= XP_011517763.1:p.Asn291=
XM_011519462.1:c.803A= XP_011517764.1:p.Asn268=
XM_011519462.2:c.803A= XP_011517764.1:p.Asn268=
XM_011519463.1:c.773A= XP_011517765.1:p.Asn258=
XM_011519463.2:c.773A= XP_011517765.1:p.Asn258=
XM_011519464.1:c.719A= XP_011517766.1:p.Asn240=
XM_011519464.2:c.719A= XP_011517766.1:p.Asn240=
XM_011519465.1:c.872A= XP_011517767.1:p.Asn291=
XM_011519466.1:c.872A= XP_011517768.1:p.Asn291=
XM_011519466.2:c.872A= XP_011517768.1:p.Asn291=
XM_011519467.1:c.650A= XP_011517769.1:p.Asn217=
XM_011519467.2:c.650A= XP_011517769.1:p.Asn217=
XM_011519468.1:c.872A= XP_011517770.1:p.Asn291=
XM_011519469.1:c.773A= XP_011517771.1:p.Asn258=
XM_011519470.1:c.551A= XP_011517772.1:p.Asn184=
XM_011519470.2:c.551A= XP_011517772.1:p.Asn184=
XM_011519471.1:c.524A= XP_011517773.1:p.Asn175=
XM_011519471.2:c.524A= XP_011517773.1:p.Asn175=
XM_011519472.1:c.455A= XP_011517774.1:p.Asn152=
XM_011519472.2:c.455A= XP_011517774.1:p.Asn152=
XM_011519473.1:c.437A= XP_011517775.1:p.Asn146=
XM_011519474.1:c.425A= XP_011517776.1:p.Asn142=
XM_011519474.2:c.425A= XP_011517776.1:p.Asn142=
XM_011519475.1:c.356A= XP_011517777.1:p.Asn119=
XM_011519475.2:c.356A= XP_011517777.1:p.Asn119=
XM_011519476.1:c.356A= XP_011517778.1:p.Asn119=
XM_011519476.2:c.356A= XP_011517778.1:p.Asn119=
XM_011519477.1:c.356A= XP_011517779.1:p.Asn119=
XM_011519477.2:c.356A= XP_011517779.1:p.Asn119=
XM_017016195.1:c.719A= XP_016871684.1:p.Asn240=
XM_017016196.1:c.437A= XP_016871685.1:p.Asn146=
XM_017016197.2:c.437A= XP_016871686.1:p.Asn146=
XM_017016198.1:c.524A= XP_016871687.1:p.Asn175=
XM_017016200.2:c.338A= XP_016871689.1:p.Asn113=
XM_024447983.1:c.437A= XP_024303751.1:p.Asn146=
XR_001747348.1:n.613T=