Canonical Allele Identifier: CA2483126594

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206770913C= , CM000663.2:g.206770913C= GRCh38
NC_000001.10:g.206944258C= , CM000663.1:g.206944258C= GRCh37
NC_000001.9:g.205010881C= NCBI36
NG_012088.1:g.6582G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.277G= (IL10)
ENST00000471071.2:c.117G= (IL10) ENSP00000493073.2:p.Arg39=
ENST00000659065.2:c.255G= (IL10) ENSP00000499588.1:p.Arg85=
ENST00000659642.2:c.255G= (IL10) ENSP00000499509.1:p.Arg85=
ENST00000664374.2:c.255G= (IL10) ENSP00000499664.1:p.Arg85=
ENST00000659997.3:c.-314C= (IL19) MANE Select ENSP00000499459.2:n.-314C=
ENST00000656872.2:c.-149+83C= (IL19) ENSP00000499487.2:n.-149+83C=
ENST00000659065.1:c.255G= (IL10) ENSP00000499588.1:p.Arg85=
ENST00000659642.1:c.255G= (IL10) ENSP00000499509.1:p.Arg85=
ENST00000659997.2:c.-314C= (IL19) ENSP00000499459.2:n.-314C=
ENST00000662320.1:n.67+83C= (IL19)
ENST00000664374.1:c.255G= (IL10) ENSP00000499664.1:p.Arg85=
ENST00000367099.3:n.277G= (IL10)
ENST00000423557.1:c.372G= (IL10) MANE Select ENSP00000412237.1:p.Arg124=
ENST00000471071.1:n.287G= (IL10)
NM_000572.2:c.372G= (IL10) NP_000563.1:p.Arg124=
XM_011509506.1:c.372G= (IL10) XP_011507808.1:p.Arg124=
NM_000572.3:c.372G= (IL10) MANE Select NP_000563.1:p.Arg124=
NM_153758.3:c.-200C= (IL19) NP_715639.1:n.-200C=
NM_001382624.1:c.117G= (IL10) NP_001369553.1:p.Arg39=
NM_001393490.1:c.-149+83C= (IL19) NP_001380419.1:n.-149+83C=
NM_153758.5:c.-314C= (IL19) MANE Select NP_715639.2:n.-314C=
NR_168466.1:n.431G= (IL10)