Canonical Allele Identifier: CA2483126507

Gene: IL10

Linked Data

• dbSNP Id: rs1674801893

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770698_206770699insC , CM000663.2:g.206770698_206770699insC	GRCh38
NC_000001.10:g.206944043_206944044insC , CM000663.1:g.206944043_206944044insC	GRCh37
NC_000001.9:g.205010666_205010667insC	NCBI36
NG_012088.1:g.6796_6797insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.283+208_283+209insG
ENST00000471071.2:c.123+208_123+209insG	ENSP00000493073.2:n.123+208_123+209insG
ENST00000659065.2:c.261+208_261+209insG	ENSP00000499588.1:n.261+208_261+209insG
ENST00000659642.2:c.261+208_261+209insG	ENSP00000499509.1:n.261+208_261+209insG
ENST00000664374.2:c.261+208_261+209insG	ENSP00000499664.1:n.261+208_261+209insG
ENST00000659065.1:c.261+208_261+209insG	ENSP00000499588.1:n.261+208_261+209insG
ENST00000659642.1:c.261+208_261+209insG	ENSP00000499509.1:n.261+208_261+209insG
ENST00000664374.1:c.261+208_261+209insG	ENSP00000499664.1:n.261+208_261+209insG
ENST00000367099.3:n.283+208_283+209insG
ENST00000423557.1:c.378+208_378+209insG MANE Select	ENSP00000412237.1:n.378+208_378+209insG
ENST00000471071.1:n.293+208_293+209insG
NM_000572.2:c.378+208_378+209insG	NP_000563.1:n.378+208_378+209insG
XM_011509506.1:c.378+208_378+209insG	XP_011507808.1:n.378+208_378+209insG
NM_000572.3:c.378+208_378+209insG MANE Select	NP_000563.1:n.378+208_378+209insG
NM_001382624.1:c.123+208_123+209insG	NP_001369553.1:n.123+208_123+209insG
NR_168466.1:n.437+208_437+209insG