Canonical Allele Identifier: CA2483126500

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770689_206770690delinsTG , CM000663.2:g.206770689_206770690delinsTG	GRCh38
NC_000001.10:g.206944034_206944035delinsTG , CM000663.1:g.206944034_206944035delinsTG	GRCh37
NC_000001.9:g.205010657_205010658delinsTG	NCBI36
NG_012088.1:g.6805_6806delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.283+217_283+218delinsCA
ENST00000471071.2:c.123+217_123+218delinsCA	ENSP00000493073.2:n.123+217_123+218delinsCA
ENST00000659065.2:c.261+217_261+218delinsCA	ENSP00000499588.1:n.261+217_261+218delinsCA
ENST00000659642.2:c.261+217_261+218delinsCA	ENSP00000499509.1:n.261+217_261+218delinsCA
ENST00000664374.2:c.261+217_261+218delinsCA	ENSP00000499664.1:n.261+217_261+218delinsCA
ENST00000659065.1:c.261+217_261+218delinsCA	ENSP00000499588.1:n.261+217_261+218delinsCA
ENST00000659642.1:c.261+217_261+218delinsCA	ENSP00000499509.1:n.261+217_261+218delinsCA
ENST00000664374.1:c.261+217_261+218delinsCA	ENSP00000499664.1:n.261+217_261+218delinsCA
ENST00000367099.3:n.283+217_283+218delinsCA
ENST00000423557.1:c.378+217_378+218delinsCA MANE Select	ENSP00000412237.1:n.378+217_378+218delinsCA
ENST00000471071.1:n.293+217_293+218delinsCA
NM_000572.2:c.378+217_378+218delinsCA	NP_000563.1:n.378+217_378+218delinsCA
XM_011509506.1:c.378+217_378+218delinsCA	XP_011507808.1:n.378+217_378+218delinsCA
NM_000572.3:c.378+217_378+218delinsCA MANE Select	NP_000563.1:n.378+217_378+218delinsCA
NM_001382624.1:c.123+217_123+218delinsCA	NP_001369553.1:n.123+217_123+218delinsCA
NR_168466.1:n.437+217_437+218delinsCA