Canonical Allele Identifier: CA2483125755

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768650T= , CM000663.2:g.206768650T=	GRCh38
NC_000001.10:g.206941995T= , CM000663.1:g.206941995T=	GRCh37
NC_000001.9:g.205008618T=	NCBI36
NG_012088.1:g.8845A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1528A=
ENST00000471071.2:c.268A=	ENSP00000493073.2:p.Lys90=
ENST00000640756.2:n.333A=
ENST00000659065.2:c.406A=	ENSP00000499588.1:p.Lys136=
ENST00000659642.2:c.406A=	ENSP00000499509.1:p.Lys136=
ENST00000664374.2:c.406A=	ENSP00000499664.1:p.Lys136=
ENST00000640756.1:n.322A=
ENST00000659065.1:c.406A=	ENSP00000499588.1:p.Lys136=
ENST00000659642.1:c.406A=	ENSP00000499509.1:p.Lys136=
ENST00000664374.1:c.406A=	ENSP00000499664.1:p.Lys136=
ENST00000423557.1:c.523A= MANE Select	ENSP00000412237.1:p.Lys175=
NM_000572.2:c.523A=	NP_000563.1:p.Lys175=
XM_011509506.1:c.523A=	XP_011507808.1:p.Lys175=
NM_000572.3:c.523A= MANE Select	NP_000563.1:p.Lys175=
NM_001382624.1:c.268A=	NP_001369553.1:p.Lys90=
NR_168466.1:n.820A=
NR_168467.1:n.350A=