Canonical Allele Identifier: CA344481612

Gene: IL10

Linked Data

• gnomAD v4: 1-206768675-G-T
• MyVariant Identifiers: chr1:g.206942020G>T (hg19) ; chr1:g.206768675G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768675G>T , CM000663.2:g.206768675G>T	GRCh38
NC_000001.10:g.206942020G>T , CM000663.1:g.206942020G>T	GRCh37
NC_000001.9:g.205008643G>T	NCBI36
NG_012088.1:g.8820C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1503C>A
ENST00000471071.2:c.243C>A	ENSP00000493073.2:p.Asn81Lys
ENST00000640756.2:n.308C>A
ENST00000659065.2:c.381C>A	ENSP00000499588.1:p.Asn127Lys
ENST00000659642.2:c.381C>A	ENSP00000499509.1:p.Asn127Lys
ENST00000664374.2:c.381C>A	ENSP00000499664.1:p.Asn127Lys
ENST00000640756.1:n.297C>A
ENST00000659065.1:c.381C>A	ENSP00000499588.1:p.Asn127Lys
ENST00000659642.1:c.381C>A	ENSP00000499509.1:p.Asn127Lys
ENST00000664374.1:c.381C>A	ENSP00000499664.1:p.Asn127Lys
ENST00000423557.1:c.498C>A MANE Select	ENSP00000412237.1:p.Asn166Lys
NM_000572.2:c.498C>A	NP_000563.1:p.Asn166Lys
XM_011509506.1:c.498C>A	XP_011507808.1:p.Asn166Lys
NM_000572.3:c.498C>A MANE Select	NP_000563.1:p.Asn166Lys
NM_001382624.1:c.243C>A	NP_001369553.1:p.Asn81Lys
NR_168466.1:n.795C>A
NR_168467.1:n.325C>A