Canonical Allele Identifier: CA2573131470

Gene: IL10 IL19

Linked Data

• ClinVar Variation Id: 1568337
• ClinVar RCV Id: RCV002210370
• dbSNP Id: rs2102439038

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770887_206770888delinsGG , CM000663.2:g.206770887_206770888delinsGG	GRCh38
NC_000001.10:g.206944232_206944233delinsGG , CM000663.1:g.206944232_206944233delinsGG	GRCh37
NC_000001.9:g.205010855_205010856delinsGG	NCBI36
NG_012088.1:g.6607_6608delinsCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.283+19_283+20delinsCC (IL10)
ENST00000471071.2:c.123+19_123+20delinsCC (IL10)	ENSP00000493073.2:n.123+19_123+20delinsCC
ENST00000659065.2:c.261+19_261+20delinsCC (IL10)	ENSP00000499588.1:n.261+19_261+20delinsCC
ENST00000659642.2:c.261+19_261+20delinsCC (IL10)	ENSP00000499509.1:n.261+19_261+20delinsCC
ENST00000664374.2:c.261+19_261+20delinsCC (IL10)	ENSP00000499664.1:n.261+19_261+20delinsCC
ENST00000659997.3:c.-340_-339delinsGG (IL19) MANE Select	ENSP00000499459.2:n.-340_-339delinsGG
ENST00000656872.2:c.-149+57_-149+58delinsGG (IL19)	ENSP00000499487.2:n.-149+57_-149+58delinsGG
ENST00000659065.1:c.261+19_261+20delinsCC (IL10)	ENSP00000499588.1:n.261+19_261+20delinsCC
ENST00000659642.1:c.261+19_261+20delinsCC (IL10)	ENSP00000499509.1:n.261+19_261+20delinsCC
ENST00000659997.2:c.-340_-339delinsGG (IL19)	ENSP00000499459.2:n.-340_-339delinsGG
ENST00000662320.1:n.67+57_67+58delinsGG (IL19)
ENST00000664374.1:c.261+19_261+20delinsCC (IL10)	ENSP00000499664.1:n.261+19_261+20delinsCC
ENST00000367099.3:n.283+19_283+20delinsCC (IL10)
ENST00000423557.1:c.378+19_378+20delinsCC (IL10) MANE Select	ENSP00000412237.1:n.378+19_378+20delinsCC
ENST00000471071.1:n.293+19_293+20delinsCC (IL10)
NM_000572.2:c.378+19_378+20delinsCC (IL10)	NP_000563.1:n.378+19_378+20delinsCC
XM_011509506.1:c.378+19_378+20delinsCC (IL10)	XP_011507808.1:n.378+19_378+20delinsCC
NM_000572.3:c.378+19_378+20delinsCC (IL10) MANE Select	NP_000563.1:n.378+19_378+20delinsCC
NM_153758.3:c.-226_-225delinsGG (IL19)	NP_715639.1:n.-226_-225delinsGG
NM_001382624.1:c.123+19_123+20delinsCC (IL10)	NP_001369553.1:n.123+19_123+20delinsCC
NM_001393490.1:c.-149+57_-149+58delinsGG (IL19)	NP_001380419.1:n.-149+57_-149+58delinsGG
NM_153758.5:c.-340_-339delinsGG (IL19) MANE Select	NP_715639.2:n.-340_-339delinsGG
NR_168466.1:n.437+19_437+20delinsCC (IL10)