Canonical Allele Identifier: CA2483125757

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768655G= , CM000663.2:g.206768655G=	GRCh38
NC_000001.10:g.206942000G= , CM000663.1:g.206942000G=	GRCh37
NC_000001.9:g.205008623G=	NCBI36
NG_012088.1:g.8840C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1523C=
ENST00000471071.2:c.263C=	ENSP00000493073.2:p.Thr88=
ENST00000640756.2:n.328C=
ENST00000659065.2:c.401C=	ENSP00000499588.1:p.Thr134=
ENST00000659642.2:c.401C=	ENSP00000499509.1:p.Thr134=
ENST00000664374.2:c.401C=	ENSP00000499664.1:p.Thr134=
ENST00000640756.1:n.317C=
ENST00000659065.1:c.401C=	ENSP00000499588.1:p.Thr134=
ENST00000659642.1:c.401C=	ENSP00000499509.1:p.Thr134=
ENST00000664374.1:c.401C=	ENSP00000499664.1:p.Thr134=
ENST00000423557.1:c.518C= MANE Select	ENSP00000412237.1:p.Thr173=
NM_000572.2:c.518C=	NP_000563.1:p.Thr173=
XM_011509506.1:c.518C=	XP_011507808.1:p.Thr173=
NM_000572.3:c.518C= MANE Select	NP_000563.1:p.Thr173=
NM_001382624.1:c.263C=	NP_001369553.1:p.Thr88=
NR_168466.1:n.815C=
NR_168467.1:n.345C=