Canonical Allele Identifier: CA2483126522

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770738C= , CM000663.2:g.206770738C=	GRCh38
NC_000001.10:g.206944083C= , CM000663.1:g.206944083C=	GRCh37
NC_000001.9:g.205010706C=	NCBI36
NG_012088.1:g.6757G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.283+169G=
ENST00000471071.2:c.123+169G=	ENSP00000493073.2:n.123+169G=
ENST00000659065.2:c.261+169G=	ENSP00000499588.1:n.261+169G=
ENST00000659642.2:c.261+169G=	ENSP00000499509.1:n.261+169G=
ENST00000664374.2:c.261+169G=	ENSP00000499664.1:n.261+169G=
ENST00000659065.1:c.261+169G=	ENSP00000499588.1:n.261+169G=
ENST00000659642.1:c.261+169G=	ENSP00000499509.1:n.261+169G=
ENST00000664374.1:c.261+169G=	ENSP00000499664.1:n.261+169G=
ENST00000367099.3:n.283+169G=
ENST00000423557.1:c.378+169G= MANE Select	ENSP00000412237.1:n.378+169G=
ENST00000471071.1:n.293+169G=
NM_000572.2:c.378+169G=	NP_000563.1:n.378+169G=
XM_011509506.1:c.378+169G=	XP_011507808.1:n.378+169G=
NM_000572.3:c.378+169G= MANE Select	NP_000563.1:n.378+169G=
NM_001382624.1:c.123+169G=	NP_001369553.1:n.123+169G=
NR_168466.1:n.437+169G=