Canonical Allele Identifier: CA2483125770

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768709T= , CM000663.2:g.206768709T=	GRCh38
NC_000001.10:g.206942054T= , CM000663.1:g.206942054T=	GRCh37
NC_000001.9:g.205008677T=	NCBI36
NG_012088.1:g.8786A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1469A=
ENST00000471071.2:c.209A=	ENSP00000493073.2:p.Tyr70=
ENST00000640756.2:n.274A=
ENST00000659065.2:c.347A=	ENSP00000499588.1:p.Tyr116=
ENST00000659642.2:c.347A=	ENSP00000499509.1:p.Tyr116=
ENST00000664374.2:c.347A=	ENSP00000499664.1:p.Tyr116=
ENST00000640756.1:n.263A=
ENST00000659065.1:c.347A=	ENSP00000499588.1:p.Tyr116=
ENST00000659642.1:c.347A=	ENSP00000499509.1:p.Tyr116=
ENST00000664374.1:c.347A=	ENSP00000499664.1:p.Tyr116=
ENST00000423557.1:c.464A= MANE Select	ENSP00000412237.1:p.Tyr155=
ENST00000471071.1:n.379A=
NM_000572.2:c.464A=	NP_000563.1:p.Tyr155=
XM_011509506.1:c.464A=	XP_011507808.1:p.Tyr155=
NM_000572.3:c.464A= MANE Select	NP_000563.1:p.Tyr155=
NM_001382624.1:c.209A=	NP_001369553.1:p.Tyr70=
NR_168466.1:n.761A=
NR_168467.1:n.291A=