Canonical Allele Identifier: CA2747495652
Gene: IL10 HGNC NCBI
IL19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771522_206771532del , CM000663.2:g.206771522_206771532del GRCh38
NC_000001.10:g.206944867_206944877del , CM000663.1:g.206944867_206944877del GRCh37
NC_000001.9:g.205011490_205011500del NCBI36
NG_012088.1:g.5963_5973del

Transcript Alleles

HGVS Amino-acid change
ENST00000659065.2:c.49-117_49-107del (IL10) ENSP00000499588.1:n.49-117_49-107del
ENST00000659642.2:c.49-117_49-107del (IL10) ENSP00000499509.1:n.49-117_49-107del
ENST00000664374.2:c.49-117_49-107del (IL10) ENSP00000499664.1:n.49-117_49-107del
ENST00000659997.3:c.-149+444_-149+454del (IL19) MANE Select ENSP00000499459.2:n.-149+444_-149+454del
ENST00000656872.2:c.-149+692_-149+702del (IL19) ENSP00000499487.2:n.-149+692_-149+702del
ENST00000659065.1:c.49-117_49-107del (IL10) ENSP00000499588.1:n.49-117_49-107del
ENST00000659642.1:c.49-117_49-107del (IL10) ENSP00000499509.1:n.49-117_49-107del
ENST00000659997.2:c.-149+444_-149+454del (IL19) ENSP00000499459.2:n.-149+444_-149+454del
ENST00000662320.1:n.67+692_67+702del (IL19)
ENST00000664374.1:c.49-117_49-107del (IL10) ENSP00000499664.1:n.49-117_49-107del
ENST00000423557.1:c.166-117_166-107del (IL10) MANE Select ENSP00000412237.1:n.166-117_166-107del
NM_000572.2:c.166-117_166-107del (IL10) NP_000563.1:n.166-117_166-107del
XM_011509506.1:c.166-117_166-107del (IL10) XP_011507808.1:n.166-117_166-107del
NM_000572.3:c.166-117_166-107del (IL10) MANE Select NP_000563.1:n.166-117_166-107del
NM_153758.3:c.-35+444_-35+454del (IL19) NP_715639.1:n.-35+444_-35+454del
NM_001393490.1:c.-149+692_-149+702del (IL19) NP_001380419.1:n.-149+692_-149+702del
NM_153758.5:c.-149+444_-149+454del (IL19) MANE Select NP_715639.2:n.-149+444_-149+454del
NR_168466.1:n.225-117_225-107del (IL10)
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