Canonical Allele Identifier: CA344481722

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942065C>A (hg19) ; chr1:g.206768720C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768720C>A , CM000663.2:g.206768720C>A	GRCh38
NC_000001.10:g.206942065C>A , CM000663.1:g.206942065C>A	GRCh37
NC_000001.9:g.205008688C>A	NCBI36
NG_012088.1:g.8775G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1458G>T
ENST00000471071.2:c.198G>T	ENSP00000493073.2:p.Glu66Asp
ENST00000640756.2:n.263G>T
ENST00000659065.2:c.336G>T	ENSP00000499588.1:p.Glu112Asp
ENST00000659642.2:c.336G>T	ENSP00000499509.1:p.Glu112Asp
ENST00000664374.2:c.336G>T	ENSP00000499664.1:p.Glu112Asp
ENST00000640756.1:n.252G>T
ENST00000659065.1:c.336G>T	ENSP00000499588.1:p.Glu112Asp
ENST00000659642.1:c.336G>T	ENSP00000499509.1:p.Glu112Asp
ENST00000664374.1:c.336G>T	ENSP00000499664.1:p.Glu112Asp
ENST00000423557.1:c.453G>T MANE Select	ENSP00000412237.1:p.Glu151Asp
ENST00000471071.1:n.368G>T
NM_000572.2:c.453G>T	NP_000563.1:p.Glu151Asp
XM_011509506.1:c.453G>T	XP_011507808.1:p.Glu151Asp
NM_000572.3:c.453G>T MANE Select	NP_000563.1:p.Glu151Asp
NM_001382624.1:c.198G>T	NP_001369553.1:p.Glu66Asp
NR_168466.1:n.750G>T
NR_168467.1:n.280G>T