Canonical Allele Identifier: CA2650217468

Gene: IL10

Linked Data

• gnomAD v4: 1-206768757-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768760_206768761del , CM000663.2:g.206768760_206768761del	GRCh38
NC_000001.10:g.206942105_206942106del , CM000663.1:g.206942105_206942106del	GRCh37
NC_000001.9:g.205008728_205008729del	NCBI36
NG_012088.1:g.8736_8737del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1419_1420del
ENST00000471071.2:c.190-31_190-30del	ENSP00000493073.2:n.190-31_190-30del
ENST00000640756.2:n.255-31_255-30del
ENST00000659065.2:c.328-31_328-30del	ENSP00000499588.1:n.328-31_328-30del
ENST00000659642.2:c.328-31_328-30del	ENSP00000499509.1:n.328-31_328-30del
ENST00000664374.2:c.328-31_328-30del	ENSP00000499664.1:n.328-31_328-30del
ENST00000640756.1:n.244-31_244-30del
ENST00000659065.1:c.328-31_328-30del	ENSP00000499588.1:n.328-31_328-30del
ENST00000659642.1:c.328-31_328-30del	ENSP00000499509.1:n.328-31_328-30del
ENST00000664374.1:c.328-31_328-30del	ENSP00000499664.1:n.328-31_328-30del
ENST00000423557.1:c.445-31_445-30del MANE Select	ENSP00000412237.1:n.445-31_445-30del
ENST00000471071.1:n.360-31_360-30del
NM_000572.2:c.445-31_445-30del	NP_000563.1:n.445-31_445-30del
XM_011509506.1:c.445-31_445-30del	XP_011507808.1:n.445-31_445-30del
NM_000572.3:c.445-31_445-30del MANE Select	NP_000563.1:n.445-31_445-30del
NM_001382624.1:c.190-31_190-30del	NP_001369553.1:n.190-31_190-30del
NR_168466.1:n.742-31_742-30del
NR_168467.1:n.272-31_272-30del