Canonical Allele Identifier: CA344481899

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206769890C>T , CM000663.2:g.206769890C>T	GRCh38
NC_000001.10:g.206943235C>T , CM000663.1:g.206943235C>T	GRCh37
NC_000001.9:g.205009858C>T	NCBI36
NG_012088.1:g.7605G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000572.3:c.383G>A MANE Select	NP_000563.1:p.Arg128Gln
ENST00000423557.1:c.383G>A MANE Select	ENSP00000412237.1:p.Arg128Gln
NM_000572.2:c.383G>A	NP_000563.1:p.Arg128Gln
NM_001382624.1:c.128G>A	NP_001369553.1:p.Arg43Gln
NR_168466.1:n.680G>A
NR_168467.1:n.210G>A
ENST00000367099.3:n.288G>A
ENST00000367099.4:n.288G>A
ENST00000471071.1:n.298G>A
ENST00000471071.2:c.128G>A	ENSP00000493073.2:p.Arg43Gln
ENST00000640756.1:n.182G>A
ENST00000640756.2:n.193G>A
ENST00000659065.1:c.266G>A	ENSP00000499588.1:p.Arg89Gln
ENST00000659065.2:c.266G>A	ENSP00000499588.1:p.Arg89Gln
ENST00000659642.1:c.266G>A	ENSP00000499509.1:p.Arg89Gln
ENST00000659642.2:c.266G>A	ENSP00000499509.1:p.Arg89Gln
ENST00000664374.1:c.266G>A	ENSP00000499664.1:p.Arg89Gln
ENST00000664374.2:c.266G>A	ENSP00000499664.1:p.Arg89Gln
XM_011509506.1:c.383G>A	XP_011507808.1:p.Arg128Gln