Canonical Allele Identifier: CA2483126879
Gene: IL10 HGNC NCBI
IL19 HGNC NCBI

Linked Data

dbSNP Id: rs1674848826
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771682_206771684del , CM000663.2:g.206771682_206771684del GRCh38
NC_000001.10:g.206945027_206945029del , CM000663.1:g.206945027_206945029del GRCh37
NC_000001.9:g.205011650_205011652del NCBI36
NG_012088.1:g.5815_5817del

Transcript Alleles

HGVS Amino-acid Change
ENST00000659065.2:c.49-265_49-263del (IL10) ENSP00000499588.1:n.49-265_49-263del
ENST00000659642.2:c.49-265_49-263del (IL10) ENSP00000499509.1:n.49-265_49-263del
ENST00000664374.2:c.49-265_49-263del (IL10) ENSP00000499664.1:n.49-265_49-263del
ENST00000659997.3:c.-149+604_-149+606del (IL19) MANE Select ENSP00000499459.2:n.-149+604_-149+606del
ENST00000656872.2:c.-149+852_-149+854del (IL19) ENSP00000499487.2:n.-149+852_-149+854del
ENST00000659065.1:c.49-265_49-263del (IL10) ENSP00000499588.1:n.49-265_49-263del
ENST00000659642.1:c.49-265_49-263del (IL10) ENSP00000499509.1:n.49-265_49-263del
ENST00000659997.2:c.-149+604_-149+606del (IL19) ENSP00000499459.2:n.-149+604_-149+606del
ENST00000662320.1:n.67+852_67+854del (IL19)
ENST00000664374.1:c.49-265_49-263del (IL10) ENSP00000499664.1:n.49-265_49-263del
ENST00000423557.1:c.166-265_166-263del (IL10) MANE Select ENSP00000412237.1:n.166-265_166-263del
NM_000572.2:c.166-265_166-263del (IL10) NP_000563.1:n.166-265_166-263del
XM_011509506.1:c.166-265_166-263del (IL10) XP_011507808.1:n.166-265_166-263del
NM_000572.3:c.166-265_166-263del (IL10) MANE Select NP_000563.1:n.166-265_166-263del
NM_153758.3:c.-35+604_-35+606del (IL19) NP_715639.1:n.-35+604_-35+606del
NM_001393490.1:c.-149+852_-149+854del (IL19) NP_001380419.1:n.-149+852_-149+854del
NM_153758.5:c.-149+604_-149+606del (IL19) MANE Select NP_715639.2:n.-149+604_-149+606del
NR_168466.1:n.225-265_225-263del (IL10)
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