Canonical Allele Identifier: CA2003307842

Gene: IL10RA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.117997802A= , CM000673.2:g.117997802A=	GRCh38
NC_000011.9:g.117868517A= , CM000673.1:g.117868517A=	GRCh37
NC_000011.8:g.117373727A=	NCBI36
NG_016275.1:g.16412A= , LRG_151:g.16412A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525467.2:n.2598-913A=
ENST00000696732.1:n.2660-913A=
ENST00000227752.8:c.811-913A= MANE Select	ENSP00000227752.4:n.811-913A=
ENST00000529924.6:n.2389-913A=
ENST00000227752.7:c.811-913A=	ENSP00000227752.3:n.811-913A=
ENST00000525467.1:n.753-913A=
ENST00000526544.5:c.*347-913A=	ENSP00000435317.1:n.*347-913A=
ENST00000529924.5:n.2389-913A=
ENST00000530178.1:n.677-913A=
ENST00000530761.5:n.1188-913A=
ENST00000533700.5:n.1018-913A=
ENST00000534574.5:c.*751-913A=	ENSP00000436328.1:n.*751-913A=
NM_001558.3:c.811-913A= , LRG_151t1:c.811-913A=	NP_001549.2:n.811-913A=
NR_026691.1:n.1018-913A=
XM_024448493.1:c.364-913A=	XP_024304261.1:n.364-913A=
NM_001558.4:c.811-913A= MANE Select	NP_001549.2:n.811-913A=
NR_026691.2:n.1015-913A=