Canonical Allele Identifier: CA1630855363
Gene: IL10RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117993348A= , CM000673.2:g.117993348A= GRCh38
NC_000011.9:g.117864063A= , CM000673.1:g.117864063A= GRCh37
NC_000011.8:g.117369273A= NCBI36
NG_016275.1:g.11958A= , LRG_151:g.11958A=

Transcript Alleles

HGVS Amino-acid Change
NM_001558.4:c.475A= MANE Select NP_001549.2:p.Ser159=
ENST00000227752.8:c.475A= MANE Select ENSP00000227752.4:p.Ser159=
NM_001558.3:c.475A= , LRG_151t1:c.475A= NP_001549.2:p.Ser159=
NR_026691.1:n.682A=
NR_026691.2:n.679A=
ENST00000227752.7:c.475A= ENSP00000227752.3:p.Ser159=
ENST00000525467.2:n.823A=
ENST00000526544.5:c.*11A= ENSP00000435317.1:n.*11A=
ENST00000529924.5:n.2053A=
ENST00000529924.6:n.2053A=
ENST00000530178.1:n.341A=
ENST00000530761.5:n.852A=
ENST00000532009.1:n.291A=
ENST00000533700.5:n.682A=
ENST00000534335.1:n.295A=
ENST00000534574.5:c.*415A= ENSP00000436328.1:n.*415A=
ENST00000696732.1:n.2324A=
XM_024448493.1:c.28A= XP_024304261.1:p.Ser10=