Canonical Allele Identifier: CA344481703

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942057A>T (hg19) ; chr1:g.206768712A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768712A>T , CM000663.2:g.206768712A>T	GRCh38
NC_000001.10:g.206942057A>T , CM000663.1:g.206942057A>T	GRCh37
NC_000001.9:g.205008680A>T	NCBI36
NG_012088.1:g.8783T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1466T>A
ENST00000471071.2:c.206T>A	ENSP00000493073.2:p.Ile69Asn
ENST00000640756.2:n.271T>A
ENST00000659065.2:c.344T>A	ENSP00000499588.1:p.Ile115Asn
ENST00000659642.2:c.344T>A	ENSP00000499509.1:p.Ile115Asn
ENST00000664374.2:c.344T>A	ENSP00000499664.1:p.Ile115Asn
ENST00000640756.1:n.260T>A
ENST00000659065.1:c.344T>A	ENSP00000499588.1:p.Ile115Asn
ENST00000659642.1:c.344T>A	ENSP00000499509.1:p.Ile115Asn
ENST00000664374.1:c.344T>A	ENSP00000499664.1:p.Ile115Asn
ENST00000423557.1:c.461T>A MANE Select	ENSP00000412237.1:p.Ile154Asn
ENST00000471071.1:n.376T>A
NM_000572.2:c.461T>A	NP_000563.1:p.Ile154Asn
XM_011509506.1:c.461T>A	XP_011507808.1:p.Ile154Asn
NM_000572.3:c.461T>A MANE Select	NP_000563.1:p.Ile154Asn
NM_001382624.1:c.206T>A	NP_001369553.1:p.Ile69Asn
NR_168466.1:n.758T>A
NR_168467.1:n.288T>A