Canonical Allele Identifier: CA2483125774

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768728G= , CM000663.2:g.206768728G=	GRCh38
NC_000001.10:g.206942073G= , CM000663.1:g.206942073G=	GRCh37
NC_000001.9:g.205008696G=	NCBI36
NG_012088.1:g.8767C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1450C=
ENST00000471071.2:c.190C=	ENSP00000493073.2:p.Leu64=
ENST00000640756.2:n.255C=
ENST00000659065.2:c.328C=	ENSP00000499588.1:p.Leu110=
ENST00000659642.2:c.328C=	ENSP00000499509.1:p.Leu110=
ENST00000664374.2:c.328C=	ENSP00000499664.1:p.Leu110=
ENST00000640756.1:n.244C=
ENST00000659065.1:c.328C=	ENSP00000499588.1:p.Leu110=
ENST00000659642.1:c.328C=	ENSP00000499509.1:p.Leu110=
ENST00000664374.1:c.328C=	ENSP00000499664.1:p.Leu110=
ENST00000423557.1:c.445C= MANE Select	ENSP00000412237.1:p.Leu149=
ENST00000471071.1:n.360C=
NM_000572.2:c.445C=	NP_000563.1:p.Leu149=
XM_011509506.1:c.445C=	XP_011507808.1:p.Leu149=
NM_000572.3:c.445C= MANE Select	NP_000563.1:p.Leu149=
NM_001382624.1:c.190C=	NP_001369553.1:p.Leu64=
NR_168466.1:n.742C=
NR_168467.1:n.272C=