Canonical Allele Identifier: CA645538033

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771016_206771040del , CM000663.2:g.206771016_206771040del GRCh38
NC_000001.10:g.206944361_206944385del , CM000663.1:g.206944361_206944385del GRCh37
NC_000001.9:g.205010984_205011008del NCBI36
NG_012088.1:g.6458_6482del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.153_177del (IL10)
ENST00000471071.2:c.-8_17del (IL10)
ENST00000659065.2:c.131_155del (IL10) ENSP00000499588.1:p.Leu44TrpfsTer4
ENST00000659642.2:c.131_155del (IL10) ENSP00000499509.1:p.Leu44TrpfsTer4
ENST00000664374.2:c.131_155del (IL10) ENSP00000499664.1:p.Leu44TrpfsTer4
ENST00000659997.3:c.-211_-187del (IL19) MANE Select ENSP00000499459.2:n.-211_-187del
ENST00000656872.2:c.-149+186_-149+210del (IL19) ENSP00000499487.2:n.-149+186_-149+210del
ENST00000659065.1:c.131_155del (IL10) ENSP00000499588.1:p.Leu44TrpfsTer4
ENST00000659642.1:c.131_155del (IL10) ENSP00000499509.1:p.Leu44TrpfsTer4
ENST00000659997.2:c.-211_-187del (IL19) ENSP00000499459.2:n.-211_-187del
ENST00000662320.1:n.67+186_67+210del (IL19)
ENST00000664374.1:c.131_155del (IL10) ENSP00000499664.1:p.Leu44TrpfsTer4
ENST00000367099.3:n.153_177del (IL10)
ENST00000423557.1:c.248_272del (IL10) MANE Select ENSP00000412237.1:p.Leu83TrpfsTer4
ENST00000471071.1:n.163_187del (IL10)
NM_000572.2:c.248_272del (IL10) NP_000563.1:p.Leu83TrpfsTer4
XM_011509506.1:c.248_272del (IL10) XP_011507808.1:p.Leu83TrpfsTer4
NM_000572.3:c.248_272del (IL10) MANE Select NP_000563.1:p.Leu83TrpfsTer4
NM_153758.3:c.-97_-73del (IL19) NP_715639.1:n.-97_-73del
NM_001382624.1:c.-8_17del (IL10)
NM_001393490.1:c.-149+186_-149+210del (IL19) NP_001380419.1:n.-149+186_-149+210del
NM_153758.5:c.-211_-187del (IL19) MANE Select NP_715639.2:n.-211_-187del
NR_168466.1:n.307_331del (IL10)