Canonical Allele Identifier: CA2003302948
Gene: IL10RA HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_001558.4:c.301C= MANE Select NP_001549.2:p.Arg101=
ENST00000227752.8:c.301C= MANE Select ENSP00000227752.4:p.Arg101=
NM_001558.3:c.301C= , LRG_151t1:c.301C= NP_001549.2:p.Arg101=
NR_026691.1:n.508C=
NR_026691.2:n.505C=
ENST00000227752.7:c.301C= ENSP00000227752.3:p.Arg101=
ENST00000525467.2:n.649C=
ENST00000526544.5:c.188+1052C= ENSP00000435317.1:n.188+1052C=
ENST00000529924.5:n.1879C=
ENST00000529924.6:n.1879C=
ENST00000530761.5:n.678C=
ENST00000531365.1:n.328C=
ENST00000533700.5:n.508C=
ENST00000534335.1:n.121C=
ENST00000534574.5:c.*241C= ENSP00000436328.1:n.*241C=
ENST00000696732.1:n.2150C=
XM_024448493.1:c.-81+1052C= XP_024304261.1:n.-81+1052C=