Canonical Allele Identifier: CA2483125773

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768722C= , CM000663.2:g.206768722C=	GRCh38
NC_000001.10:g.206942067C= , CM000663.1:g.206942067C=	GRCh37
NC_000001.9:g.205008690C=	NCBI36
NG_012088.1:g.8773G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1456G=
ENST00000471071.2:c.196G=	ENSP00000493073.2:p.Glu66=
ENST00000640756.2:n.261G=
ENST00000659065.2:c.334G=	ENSP00000499588.1:p.Glu112=
ENST00000659642.2:c.334G=	ENSP00000499509.1:p.Glu112=
ENST00000664374.2:c.334G=	ENSP00000499664.1:p.Glu112=
ENST00000640756.1:n.250G=
ENST00000659065.1:c.334G=	ENSP00000499588.1:p.Glu112=
ENST00000659642.1:c.334G=	ENSP00000499509.1:p.Glu112=
ENST00000664374.1:c.334G=	ENSP00000499664.1:p.Glu112=
ENST00000423557.1:c.451G= MANE Select	ENSP00000412237.1:p.Glu151=
ENST00000471071.1:n.366G=
NM_000572.2:c.451G=	NP_000563.1:p.Glu151=
XM_011509506.1:c.451G=	XP_011507808.1:p.Glu151=
NM_000572.3:c.451G= MANE Select	NP_000563.1:p.Glu151=
NM_001382624.1:c.196G=	NP_001369553.1:p.Glu66=
NR_168466.1:n.748G=
NR_168467.1:n.278G=