Canonical Allele Identifier: CA1011578357
Gene: IL10 HGNC NCBI
IL19 HGNC NCBI

Linked Data

dbSNP Id: rs1674860242
gnomAD v3: 1-206771977-TCTC-T
gnomAD v4: 1-206771977-TCTC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771980_206771982del , CM000663.2:g.206771980_206771982del GRCh38
NC_000001.10:g.206945325_206945327del , CM000663.1:g.206945325_206945327del GRCh37
NC_000001.9:g.205011948_205011950del NCBI36
NG_012088.1:g.5515_5517del

Transcript Alleles

HGVS Amino-acid change
ENST00000659065.2:c.48+291_48+293del (IL10) ENSP00000499588.1:n.48+291_48+293del
ENST00000659642.2:c.48+291_48+293del (IL10) ENSP00000499509.1:n.48+291_48+293del
ENST00000664374.2:c.48+291_48+293del (IL10) ENSP00000499664.1:n.48+291_48+293del
ENST00000659997.3:c.-149+902_-149+904del (IL19) MANE Select ENSP00000499459.2:n.-149+902_-149+904del
ENST00000656872.2:c.-149+1150_-149+1152del (IL19) ENSP00000499487.2:n.-149+1150_-149+1152de...
ENST00000659065.1:c.48+291_48+293del (IL10) ENSP00000499588.1:n.48+291_48+293del
ENST00000659642.1:c.48+291_48+293del (IL10) ENSP00000499509.1:n.48+291_48+293del
ENST00000659997.2:c.-149+902_-149+904del (IL19) ENSP00000499459.2:n.-149+902_-149+904del
ENST00000662320.1:n.67+1150_67+1152del (IL19)
ENST00000664374.1:c.48+291_48+293del (IL10) ENSP00000499664.1:n.48+291_48+293del
ENST00000423557.1:c.165+291_165+293del (IL10) MANE Select ENSP00000412237.1:n.165+291_165+293del
NM_000572.2:c.165+291_165+293del (IL10) NP_000563.1:n.165+291_165+293del
XM_011509506.1:c.165+291_165+293del (IL10) XP_011507808.1:n.165+291_165+293del
NM_000572.3:c.165+291_165+293del (IL10) MANE Select NP_000563.1:n.165+291_165+293del
NM_153758.3:c.-35+902_-35+904del (IL19) NP_715639.1:n.-35+902_-35+904del
NM_001393490.1:c.-149+1150_-149+1152del (IL19) NP_001380419.1:n.-149+1150_-149+1152del
NM_153758.5:c.-149+902_-149+904del (IL19) MANE Select NP_715639.2:n.-149+902_-149+904del
NR_168466.1:n.224+291_224+293del (IL10)
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