Canonical Allele Identifier: CA1141846154

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768663G= , CM000663.2:g.206768663G=	GRCh38
NC_000001.10:g.206942008G= , CM000663.1:g.206942008G=	GRCh37
NC_000001.9:g.205008631G=	NCBI36
NG_012088.1:g.8832C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1515C=
ENST00000471071.2:c.255C=	ENSP00000493073.2:p.Ala85=
ENST00000640756.2:n.320C=
ENST00000659065.2:c.393C=	ENSP00000499588.1:p.Ala131=
ENST00000659642.2:c.393C=	ENSP00000499509.1:p.Ala131=
ENST00000664374.2:c.393C=	ENSP00000499664.1:p.Ala131=
ENST00000640756.1:n.309C=
ENST00000659065.1:c.393C=	ENSP00000499588.1:p.Ala131=
ENST00000659642.1:c.393C=	ENSP00000499509.1:p.Ala131=
ENST00000664374.1:c.393C=	ENSP00000499664.1:p.Ala131=
ENST00000423557.1:c.510C= MANE Select	ENSP00000412237.1:p.Ala170=
NM_000572.2:c.510C=	NP_000563.1:p.Ala170=
XM_011509506.1:c.510C=	XP_011507808.1:p.Ala170=
NM_000572.3:c.510C= MANE Select	NP_000563.1:p.Ala170=
NM_001382624.1:c.255C=	NP_001369553.1:p.Ala85=
NR_168466.1:n.807C=
NR_168467.1:n.337C=