Canonical Allele Identifier: CA130286
Gene: IL10RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117989554C>T , CM000673.2:g.117989554C>T GRCh38
NC_000011.9:g.117860269C>T , CM000673.1:g.117860269C>T GRCh37
NC_000011.8:g.117365479C>T NCBI36
NG_016275.1:g.8164C>T , LRG_151:g.8164C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001558.4:c.301C>T MANE Select NP_001549.2:p.Arg101Trp
ENST00000227752.8:c.301C>T MANE Select ENSP00000227752.4:p.Arg101Trp
NM_001558.3:c.301C>T , LRG_151t1:c.301C>T NP_001549.2:p.Arg101Trp
NR_026691.1:n.508C>T
NR_026691.2:n.505C>T
ENST00000227752.7:c.301C>T ENSP00000227752.3:p.Arg101Trp
ENST00000525467.2:n.649C>T
ENST00000526544.5:c.188+1052C>T ENSP00000435317.1:n.188+1052C>T
ENST00000529924.5:n.1879C>T
ENST00000529924.6:n.1879C>T
ENST00000530761.5:n.678C>T
ENST00000531365.1:n.328C>T
ENST00000533700.5:n.508C>T
ENST00000534335.1:n.121C>T
ENST00000534574.5:c.*241C>T ENSP00000436328.1:n.*241C>T
ENST00000696732.1:n.2150C>T
XM_024448493.1:c.-81+1052C>T XP_024304261.1:n.-81+1052C>T