Canonical Allele Identifier: CA2650217520
Gene: IL10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206768815_206768816insGGGA , CM000663.2:g.206768815_206768816insGGGA GRCh38
NC_000001.10:g.206942160_206942161insGGGA , CM000663.1:g.206942160_206942161insGGGA GRCh37
NC_000001.9:g.205008783_205008784insGGGA NCBI36
NG_012088.1:g.8681_8682insCCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.1364_1365insCCTC
ENST00000471071.2:c.190-86_190-85insCCTC ENSP00000493073.2:n.190-86_190-85insCCTC
ENST00000640756.2:n.255-86_255-85insCCTC
ENST00000659065.2:c.328-86_328-85insCCTC ENSP00000499588.1:n.328-86_328-85insCCTC
ENST00000659642.2:c.328-86_328-85insCCTC ENSP00000499509.1:n.328-86_328-85insCCTC
ENST00000664374.2:c.328-86_328-85insCCTC ENSP00000499664.1:n.328-86_328-85insCCTC
ENST00000640756.1:n.244-86_244-85insCCTC
ENST00000659065.1:c.328-86_328-85insCCTC ENSP00000499588.1:n.328-86_328-85insCCTC
ENST00000659642.1:c.328-86_328-85insCCTC ENSP00000499509.1:n.328-86_328-85insCCTC
ENST00000664374.1:c.328-86_328-85insCCTC ENSP00000499664.1:n.328-86_328-85insCCTC
ENST00000423557.1:c.445-86_445-85insCCTC MANE Select ENSP00000412237.1:n.445-86_445-85insCCTC
ENST00000471071.1:n.360-86_360-85insCCTC
NM_000572.2:c.445-86_445-85insCCTC NP_000563.1:n.445-86_445-85insCCTC
XM_011509506.1:c.445-86_445-85insCCTC XP_011507808.1:n.445-86_445-85insCCTC
NM_000572.3:c.445-86_445-85insCCTC MANE Select NP_000563.1:n.445-86_445-85insCCTC
NM_001382624.1:c.190-86_190-85insCCTC NP_001369553.1:n.190-86_190-85insCCTC
NR_168466.1:n.742-86_742-85insCCTC
NR_168467.1:n.272-86_272-85insCCTC