Canonical Allele Identifier: CA344481599

Gene: IL10

Linked Data

• ClinVar Variation Id: 1999433
• ClinVar RCV Id: RCV002819598
• MyVariant Identifiers: chr1:g.206942015A>T (hg19) ; chr1:g.206768670A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768670A>T , CM000663.2:g.206768670A>T	GRCh38
NC_000001.10:g.206942015A>T , CM000663.1:g.206942015A>T	GRCh37
NC_000001.9:g.205008638A>T	NCBI36
NG_012088.1:g.8825T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1508T>A
ENST00000471071.2:c.248T>A	ENSP00000493073.2:p.Ile83Lys
ENST00000640756.2:n.313T>A
ENST00000659065.2:c.386T>A	ENSP00000499588.1:p.Ile129Lys
ENST00000659642.2:c.386T>A	ENSP00000499509.1:p.Ile129Lys
ENST00000664374.2:c.386T>A	ENSP00000499664.1:p.Ile129Lys
ENST00000640756.1:n.302T>A
ENST00000659065.1:c.386T>A	ENSP00000499588.1:p.Ile129Lys
ENST00000659642.1:c.386T>A	ENSP00000499509.1:p.Ile129Lys
ENST00000664374.1:c.386T>A	ENSP00000499664.1:p.Ile129Lys
ENST00000423557.1:c.503T>A MANE Select	ENSP00000412237.1:p.Ile168Lys
NM_000572.2:c.503T>A	NP_000563.1:p.Ile168Lys
XM_011509506.1:c.503T>A	XP_011507808.1:p.Ile168Lys
NM_000572.3:c.503T>A MANE Select	NP_000563.1:p.Ile168Lys
NM_001382624.1:c.248T>A	NP_001369553.1:p.Ile83Lys
NR_168466.1:n.800T>A
NR_168467.1:n.330T>A