Canonical Allele Identifier: CA2650217436

Gene: IL10

Linked Data

• gnomAD v4: 1-206768716-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768719del , CM000663.2:g.206768719del	GRCh38
NC_000001.10:g.206942064del , CM000663.1:g.206942064del	GRCh37
NC_000001.9:g.205008687del	NCBI36
NG_012088.1:g.8778del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1461del
ENST00000471071.2:c.201del	ENSP00000493073.2:p.Gly68AlafsTer6
ENST00000640756.2:n.266del
ENST00000659065.2:c.339del	ENSP00000499588.1:p.Gly114AlafsTer6
ENST00000659642.2:c.339del	ENSP00000499509.1:p.Gly114AlafsTer6
ENST00000664374.2:c.339del	ENSP00000499664.1:p.Gly114AlafsTer6
ENST00000640756.1:n.255del
ENST00000659065.1:c.339del	ENSP00000499588.1:p.Gly114AlafsTer6
ENST00000659642.1:c.339del	ENSP00000499509.1:p.Gly114AlafsTer6
ENST00000664374.1:c.339del	ENSP00000499664.1:p.Gly114AlafsTer6
ENST00000423557.1:c.456del MANE Select	ENSP00000412237.1:p.Gly153AlafsTer6
ENST00000471071.1:n.371del
NM_000572.2:c.456del	NP_000563.1:p.Gly153AlafsTer6
XM_011509506.1:c.456del	XP_011507808.1:p.Gly153AlafsTer6
NM_000572.3:c.456del MANE Select	NP_000563.1:p.Gly153AlafsTer6
NM_001382624.1:c.201del	NP_001369553.1:p.Gly68AlafsTer6
NR_168466.1:n.753del
NR_168467.1:n.283del