Canonical Allele Identifier: CA229450750

Gene: IL10RA SMIM35

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118001371G>T , CM000673.2:g.118001371G>T	GRCh38
NC_000011.9:g.117872086G>T , CM000673.1:g.117872086G>T	GRCh37
NC_000011.8:g.117377296G>T	NCBI36
NG_016275.1:g.19981G>T , LRG_151:g.19981G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525467.2:n.5254G>T (IL10RA)
ENST00000696732.1:n.5316G>T (IL10RA)
ENST00000227752.8:c.*1730G>T (IL10RA) MANE Select	ENSP00000227752.4:n.*1730G>T
ENST00000529924.6:n.5045G>T (IL10RA)
ENST00000227752.7:c.*1730G>T (IL10RA)	ENSP00000227752.3:n.*1730G>T
ENST00000529924.5:n.5045G>T (IL10RA)
NM_001558.3:c.*1730G>T , LRG_151t1:c.*1730G>T (IL10RA)	NP_001549.2:n.*1730G>T
NR_026691.1:n.3674G>T (IL10RA)
XM_024448283.1:c.*5039C>A (SMIM35)	XP_024304051.1:n.*5039C>A
XM_024448493.1:c.*1730G>T (IL10RA)	XP_024304261.1:n.*1730G>T
XR_002957112.1:n.5693C>A (SMIM35)
XR_002957113.1:n.5209C>A (SMIM35)
NM_001558.4:c.*1730G>T (IL10RA) MANE Select	NP_001549.2:n.*1730G>T
NR_026691.2:n.3671G>T (IL10RA)