Canonical Allele Identifier: CA2697948484
Gene: IL10 HGNC NCBI
IL19 HGNC NCBI

Linked Data

dbSNP Id: rs2102441655
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206773001del , CM000663.2:g.206773001del GRCh38
NC_000001.10:g.206946346del , CM000663.1:g.206946346del GRCh37
NC_000001.9:g.205012969del NCBI36
NG_012088.1:g.4496del

Transcript Alleles

HGVS Amino-acid change
ENST00000659065.2:c.-14-667del (IL10) ENSP00000499588.1:n.-14-667del
ENST00000659642.2:c.-681del (IL10) ENSP00000499509.1:n.-681del
ENST00000664374.2:c.-14-667del (IL10) ENSP00000499664.1:n.-14-667del
ENST00000659997.3:c.-149+1923del (IL19) MANE Select ENSP00000499459.2:n.-149+1923del
ENST00000656872.2:c.-149+2171del (IL19) ENSP00000499487.2:n.-149+2171del
ENST00000659065.1:c.-14-667del (IL10) ENSP00000499588.1:n.-14-667del
ENST00000659642.1:c.-681del (IL10) ENSP00000499509.1:n.-681del
ENST00000659997.2:c.-149+1923del (IL19) ENSP00000499459.2:n.-149+1923del
ENST00000662320.1:n.67+2171del (IL19)
ENST00000664374.1:c.-14-667del (IL10) ENSP00000499664.1:n.-14-667del
XM_011509506.1:c.-564del (IL10) XP_011507808.1:n.-564del
NM_153758.3:c.-35+1923del (IL19) NP_715639.1:n.-35+1923del
NM_001393490.1:c.-149+2171del (IL19) NP_001380419.1:n.-149+2171del
NM_153758.5:c.-149+1923del (IL19) MANE Select NP_715639.2:n.-149+1923del
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