Canonical Allele Identifier: CA2483125797

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768814G= , CM000663.2:g.206768814G=	GRCh38
NC_000001.10:g.206942159G= , CM000663.1:g.206942159G=	GRCh37
NC_000001.9:g.205008782G=	NCBI36
NG_012088.1:g.8681C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1364C=
ENST00000471071.2:c.190-86C=	ENSP00000493073.2:n.190-86C=
ENST00000640756.2:n.255-86C=
ENST00000659065.2:c.328-86C=	ENSP00000499588.1:n.328-86C=
ENST00000659642.2:c.328-86C=	ENSP00000499509.1:n.328-86C=
ENST00000664374.2:c.328-86C=	ENSP00000499664.1:n.328-86C=
ENST00000640756.1:n.244-86C=
ENST00000659065.1:c.328-86C=	ENSP00000499588.1:n.328-86C=
ENST00000659642.1:c.328-86C=	ENSP00000499509.1:n.328-86C=
ENST00000664374.1:c.328-86C=	ENSP00000499664.1:n.328-86C=
ENST00000423557.1:c.445-86C= MANE Select	ENSP00000412237.1:n.445-86C=
ENST00000471071.1:n.360-86C=
NM_000572.2:c.445-86C=	NP_000563.1:n.445-86C=
XM_011509506.1:c.445-86C=	XP_011507808.1:n.445-86C=
NM_000572.3:c.445-86C= MANE Select	NP_000563.1:n.445-86C=
NM_001382624.1:c.190-86C=	NP_001369553.1:n.190-86C=
NR_168466.1:n.742-86C=
NR_168467.1:n.272-86C=