Canonical Allele Identifier: CA382772553

Gene: IL10RA

Linked Data

• MyVariant Identifiers: chr11:g.117859104G>C (hg19) ; chr11:g.117988389G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.117988389G>C , CM000673.2:g.117988389G>C	GRCh38
NC_000011.9:g.117859104G>C , CM000673.1:g.117859104G>C	GRCh37
NC_000011.8:g.117364314G>C	NCBI36
NG_016275.1:g.6999G>C , LRG_151:g.6999G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525467.2:n.423G>C
ENST00000696732.1:n.1924G>C
ENST00000227752.8:c.75G>C MANE Select	ENSP00000227752.4:p.Glu25Asp
ENST00000529924.6:n.1653G>C
ENST00000227752.7:c.75G>C	ENSP00000227752.3:p.Glu25Asp
ENST00000526544.5:c.75G>C	ENSP00000435317.1:p.Glu25Asp
ENST00000529924.5:n.1653G>C
ENST00000530761.5:n.452G>C
ENST00000531365.1:n.102G>C
ENST00000533700.5:n.282G>C
ENST00000534574.5:c.*15G>C	ENSP00000436328.1:n.*15G>C
NM_001558.3:c.75G>C , LRG_151t1:c.75G>C	NP_001549.2:p.Glu25Asp
NR_026691.1:n.282G>C
XM_024448493.1:c.-194G>C	XP_024304261.1:n.-194G>C
NM_001558.4:c.75G>C MANE Select	NP_001549.2:p.Glu25Asp
NR_026691.2:n.279G>C