Canonical Allele Identifier: CA2483125758

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768657C= , CM000663.2:g.206768657C=	GRCh38
NC_000001.10:g.206942002C= , CM000663.1:g.206942002C=	GRCh37
NC_000001.9:g.205008625C=	NCBI36
NG_012088.1:g.8838G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1521G=
ENST00000471071.2:c.261G=	ENSP00000493073.2:p.Met87=
ENST00000640756.2:n.326G=
ENST00000659065.2:c.399G=	ENSP00000499588.1:p.Met133=
ENST00000659642.2:c.399G=	ENSP00000499509.1:p.Met133=
ENST00000664374.2:c.399G=	ENSP00000499664.1:p.Met133=
ENST00000640756.1:n.315G=
ENST00000659065.1:c.399G=	ENSP00000499588.1:p.Met133=
ENST00000659642.1:c.399G=	ENSP00000499509.1:p.Met133=
ENST00000664374.1:c.399G=	ENSP00000499664.1:p.Met133=
ENST00000423557.1:c.516G= MANE Select	ENSP00000412237.1:p.Met172=
NM_000572.2:c.516G=	NP_000563.1:p.Met172=
XM_011509506.1:c.516G=	XP_011507808.1:p.Met172=
NM_000572.3:c.516G= MANE Select	NP_000563.1:p.Met172=
NM_001382624.1:c.261G=	NP_001369553.1:p.Met87=
NR_168466.1:n.813G=
NR_168467.1:n.343G=