Canonical Allele Identifier: CA2650217473

Gene: IL10

Linked Data

• gnomAD v4: 1-206768764-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768766_206768767del , CM000663.2:g.206768766_206768767del	GRCh38
NC_000001.10:g.206942111_206942112del , CM000663.1:g.206942111_206942112del	GRCh37
NC_000001.9:g.205008734_205008735del	NCBI36
NG_012088.1:g.8729_8730del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1412_1413del
ENST00000471071.2:c.190-38_190-37del	ENSP00000493073.2:n.190-38_190-37del
ENST00000640756.2:n.255-38_255-37del
ENST00000659065.2:c.328-38_328-37del	ENSP00000499588.1:n.328-38_328-37del
ENST00000659642.2:c.328-38_328-37del	ENSP00000499509.1:n.328-38_328-37del
ENST00000664374.2:c.328-38_328-37del	ENSP00000499664.1:n.328-38_328-37del
ENST00000640756.1:n.244-38_244-37del
ENST00000659065.1:c.328-38_328-37del	ENSP00000499588.1:n.328-38_328-37del
ENST00000659642.1:c.328-38_328-37del	ENSP00000499509.1:n.328-38_328-37del
ENST00000664374.1:c.328-38_328-37del	ENSP00000499664.1:n.328-38_328-37del
ENST00000423557.1:c.445-38_445-37del MANE Select	ENSP00000412237.1:n.445-38_445-37del
ENST00000471071.1:n.360-38_360-37del
NM_000572.2:c.445-38_445-37del	NP_000563.1:n.445-38_445-37del
XM_011509506.1:c.445-38_445-37del	XP_011507808.1:n.445-38_445-37del
NM_000572.3:c.445-38_445-37del MANE Select	NP_000563.1:n.445-38_445-37del
NM_001382624.1:c.190-38_190-37del	NP_001369553.1:n.190-38_190-37del
NR_168466.1:n.742-38_742-37del
NR_168467.1:n.272-38_272-37del