Canonical Allele Identifier: CA344481548

Gene: IL10

Linked Data

• gnomAD v4: 1-206768648-C-G
• MyVariant Identifiers: chr1:g.206941993C>G (hg19) ; chr1:g.206768648C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768648C>G , CM000663.2:g.206768648C>G	GRCh38
NC_000001.10:g.206941993C>G , CM000663.1:g.206941993C>G	GRCh37
NC_000001.9:g.205008616C>G	NCBI36
NG_012088.1:g.8847G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1530G>C
ENST00000471071.2:c.270G>C	ENSP00000493073.2:p.Lys90Asn
ENST00000640756.2:n.335G>C
ENST00000659065.2:c.408G>C	ENSP00000499588.1:p.Lys136Asn
ENST00000659642.2:c.408G>C	ENSP00000499509.1:p.Lys136Asn
ENST00000664374.2:c.408G>C	ENSP00000499664.1:p.Lys136Asn
ENST00000640756.1:n.324G>C
ENST00000659065.1:c.408G>C	ENSP00000499588.1:p.Lys136Asn
ENST00000659642.1:c.408G>C	ENSP00000499509.1:p.Lys136Asn
ENST00000664374.1:c.408G>C	ENSP00000499664.1:p.Lys136Asn
ENST00000423557.1:c.525G>C MANE Select	ENSP00000412237.1:p.Lys175Asn
NM_000572.2:c.525G>C	NP_000563.1:p.Lys175Asn
XM_011509506.1:c.525G>C	XP_011507808.1:p.Lys175Asn
NM_000572.3:c.525G>C MANE Select	NP_000563.1:p.Lys175Asn
NM_001382624.1:c.270G>C	NP_001369553.1:p.Lys90Asn
NR_168466.1:n.822G>C
NR_168467.1:n.352G>C