Canonical Allele Identifier: CA2697953154
Gene: IL10 HGNC NCBI
IL19 HGNC NCBI

Linked Data

dbSNP Id: rs2102440312
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771843_206771859del , CM000663.2:g.206771843_206771859del GRCh38
NC_000001.10:g.206945188_206945204del , CM000663.1:g.206945188_206945204del GRCh37
NC_000001.9:g.205011811_205011827del NCBI36
NG_012088.1:g.5638_5654del

Transcript Alleles

HGVS Amino-acid Change
ENST00000659065.2:c.48+414_49-426del (IL10) ENSP00000499588.1:n.48+414_49-426del
ENST00000659642.2:c.48+414_49-426del (IL10) ENSP00000499509.1:n.48+414_49-426del
ENST00000664374.2:c.48+414_49-426del (IL10) ENSP00000499664.1:n.48+414_49-426del
ENST00000659997.3:c.-149+765_-149+781del (IL19) MANE Select ENSP00000499459.2:n.-149+765_-149+781del
ENST00000656872.2:c.-149+1013_-149+1029del (IL19) ENSP00000499487.2:n.-149+1013_-149+1029del
ENST00000659065.1:c.48+414_49-426del (IL10) ENSP00000499588.1:n.48+414_49-426del
ENST00000659642.1:c.48+414_49-426del (IL10) ENSP00000499509.1:n.48+414_49-426del
ENST00000659997.2:c.-149+765_-149+781del (IL19) ENSP00000499459.2:n.-149+765_-149+781del
ENST00000662320.1:n.67+1013_67+1029del (IL19)
ENST00000664374.1:c.48+414_49-426del (IL10) ENSP00000499664.1:n.48+414_49-426del
ENST00000423557.1:c.165+414_166-426del (IL10) MANE Select ENSP00000412237.1:n.165+414_166-426del
NM_000572.2:c.165+414_166-426del (IL10) NP_000563.1:n.165+414_166-426del
XM_011509506.1:c.165+414_166-426del (IL10) XP_011507808.1:n.165+414_166-426del
NM_000572.3:c.165+414_166-426del (IL10) MANE Select NP_000563.1:n.165+414_166-426del
NM_153758.3:c.-35+765_-35+781del (IL19) NP_715639.1:n.-35+765_-35+781del
NM_001393490.1:c.-149+1013_-149+1029del (IL19) NP_001380419.1:n.-149+1013_-149+1029del
NM_153758.5:c.-149+765_-149+781del (IL19) MANE Select NP_715639.2:n.-149+765_-149+781del
NR_168466.1:n.224+414_225-426del (IL10)
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