Canonical Allele Identifier: CA2483126523

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770740_206770742delinsCAA , CM000663.2:g.206770740_206770742delinsCAA	GRCh38
NC_000001.10:g.206944085_206944087delinsCAA , CM000663.1:g.206944085_206944087delinsCAA	GRCh37
NC_000001.9:g.205010708_205010710delinsCAA	NCBI36
NG_012088.1:g.6753_6755delinsTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.283+165_283+167delinsTTG
ENST00000471071.2:c.123+165_123+167delinsTTG	ENSP00000493073.2:n.123+165_123+167delinsTTG
ENST00000659065.2:c.261+165_261+167delinsTTG	ENSP00000499588.1:n.261+165_261+167delinsTTG
ENST00000659642.2:c.261+165_261+167delinsTTG	ENSP00000499509.1:n.261+165_261+167delinsTTG
ENST00000664374.2:c.261+165_261+167delinsTTG	ENSP00000499664.1:n.261+165_261+167delinsTTG
ENST00000659065.1:c.261+165_261+167delinsTTG	ENSP00000499588.1:n.261+165_261+167delinsTTG
ENST00000659642.1:c.261+165_261+167delinsTTG	ENSP00000499509.1:n.261+165_261+167delinsTTG
ENST00000664374.1:c.261+165_261+167delinsTTG	ENSP00000499664.1:n.261+165_261+167delinsTTG
ENST00000367099.3:n.283+165_283+167delinsTTG
ENST00000423557.1:c.378+165_378+167delinsTTG MANE Select	ENSP00000412237.1:n.378+165_378+167delinsTTG
ENST00000471071.1:n.293+165_293+167delinsTTG
NM_000572.2:c.378+165_378+167delinsTTG	NP_000563.1:n.378+165_378+167delinsTTG
XM_011509506.1:c.378+165_378+167delinsTTG	XP_011507808.1:n.378+165_378+167delinsTTG
NM_000572.3:c.378+165_378+167delinsTTG MANE Select	NP_000563.1:n.378+165_378+167delinsTTG
NM_001382624.1:c.123+165_123+167delinsTTG	NP_001369553.1:n.123+165_123+167delinsTTG
NR_168466.1:n.437+165_437+167delinsTTG