Canonical Allele Identifier: CA2483125873

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206769016_206769017delinsAT , CM000663.2:g.206769016_206769017delinsAT	GRCh38
NC_000001.10:g.206942361_206942362delinsAT , CM000663.1:g.206942361_206942362delinsAT	GRCh37
NC_000001.9:g.205008984_205008985delinsAT	NCBI36
NG_012088.1:g.8478_8479delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.1161_1162delinsAT
ENST00000471071.2:c.190-289_190-288delinsAT	ENSP00000493073.2:n.190-289_190-288delins...
ENST00000640756.2:n.255-289_255-288delinsAT
ENST00000659065.2:c.328-289_328-288delinsAT	ENSP00000499588.1:n.328-289_328-288delins...
ENST00000659642.2:c.328-289_328-288delinsAT	ENSP00000499509.1:n.328-289_328-288delins...
ENST00000664374.2:c.328-289_328-288delinsAT	ENSP00000499664.1:n.328-289_328-288delins...
ENST00000640756.1:n.244-289_244-288delinsAT
ENST00000659065.1:c.328-289_328-288delinsAT	ENSP00000499588.1:n.328-289_328-288delins...
ENST00000659642.1:c.328-289_328-288delinsAT	ENSP00000499509.1:n.328-289_328-288delins...
ENST00000664374.1:c.328-289_328-288delinsAT	ENSP00000499664.1:n.328-289_328-288delins...
ENST00000423557.1:c.445-289_445-288delinsAT MANE Select	ENSP00000412237.1:n.445-289_445-288delins...
ENST00000471071.1:n.360-289_360-288delinsAT
NM_000572.2:c.445-289_445-288delinsAT	NP_000563.1:n.445-289_445-288delinsAT
XM_011509506.1:c.445-289_445-288delinsAT	XP_011507808.1:n.445-289_445-288delinsAT
NM_000572.3:c.445-289_445-288delinsAT MANE Select	NP_000563.1:n.445-289_445-288delinsAT
NM_001382624.1:c.190-289_190-288delinsAT	NP_001369553.1:n.190-289_190-288delinsAT
NR_168466.1:n.742-289_742-288delinsAT
NR_168467.1:n.272-289_272-288delinsAT