Canonical Allele Identifier: CA2483126514

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770723_206770730delinsCACCCCCA , CM000663.2:g.206770723_206770730delinsCACCCCCA	GRCh38
NC_000001.10:g.206944068_206944075delinsCACCCCCA , CM000663.1:g.206944068_206944075delinsCACCCCCA	GRCh37
NC_000001.9:g.205010691_205010698delinsCACCCCCA	NCBI36
NG_012088.1:g.6765_6772delinsTGGGGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.283+177_283+184delinsTGGGGGTG
ENST00000471071.2:c.123+177_123+184delinsTGGGGGTG	ENSP00000493073.2:n.123+177_123+184delinsTGGGGGTG
ENST00000659065.2:c.261+177_261+184delinsTGGGGGTG	ENSP00000499588.1:n.261+177_261+184delinsTGGGGGTG
ENST00000659642.2:c.261+177_261+184delinsTGGGGGTG	ENSP00000499509.1:n.261+177_261+184delinsTGGGGGTG
ENST00000664374.2:c.261+177_261+184delinsTGGGGGTG	ENSP00000499664.1:n.261+177_261+184delinsTGGGGGTG
ENST00000659065.1:c.261+177_261+184delinsTGGGGGTG	ENSP00000499588.1:n.261+177_261+184delinsTGGGGGTG
ENST00000659642.1:c.261+177_261+184delinsTGGGGGTG	ENSP00000499509.1:n.261+177_261+184delinsTGGGGGTG
ENST00000664374.1:c.261+177_261+184delinsTGGGGGTG	ENSP00000499664.1:n.261+177_261+184delinsTGGGGGTG
ENST00000367099.3:n.283+177_283+184delinsTGGGGGTG
ENST00000423557.1:c.378+177_378+184delinsTGGGGGTG MANE Select	ENSP00000412237.1:n.378+177_378+184delinsTGGGGGTG
ENST00000471071.1:n.293+177_293+184delinsTGGGGGTG
NM_000572.2:c.378+177_378+184delinsTGGGGGTG	NP_000563.1:n.378+177_378+184delinsTGGGGGTG
XM_011509506.1:c.378+177_378+184delinsTGGGGGTG	XP_011507808.1:n.378+177_378+184delinsTGGGGGTG
NM_000572.3:c.378+177_378+184delinsTGGGGGTG MANE Select	NP_000563.1:n.378+177_378+184delinsTGGGGGTG
NM_001382624.1:c.123+177_123+184delinsTGGGGGTG	NP_001369553.1:n.123+177_123+184delinsTGGGGGTG
NR_168466.1:n.437+177_437+184delinsTGGGGGTG