Canonical Allele Identifier: CA730536551

Gene: IL10

Linked Data

• dbSNP Id: rs1261517955
• gnomAD v3: 1-206768996-G-GGTCAC
• gnomAD v4: 1-206768996-G-GGTCAC
• MyVariant Identifiers: chr1:g.206942341_206942342insGTCAC (hg19) ; chr1:g.206768996_206768997insGTCAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768999_206769003dup , CM000663.2:g.206768999_206769003dup	GRCh38
NC_000001.10:g.206942344_206942348dup , CM000663.1:g.206942344_206942348dup	GRCh37
NC_000001.9:g.205008967_205008971dup	NCBI36
NG_012088.1:g.8494_8498dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.1177_1181dup
ENST00000471071.2:c.190-273_190-269dup	ENSP00000493073.2:n.190-273_190-269dup
ENST00000640756.2:n.255-273_255-269dup
ENST00000659065.2:c.328-273_328-269dup	ENSP00000499588.1:n.328-273_328-269dup
ENST00000659642.2:c.328-273_328-269dup	ENSP00000499509.1:n.328-273_328-269dup
ENST00000664374.2:c.328-273_328-269dup	ENSP00000499664.1:n.328-273_328-269dup
ENST00000640756.1:n.244-273_244-269dup
ENST00000659065.1:c.328-273_328-269dup	ENSP00000499588.1:n.328-273_328-269dup
ENST00000659642.1:c.328-273_328-269dup	ENSP00000499509.1:n.328-273_328-269dup
ENST00000664374.1:c.328-273_328-269dup	ENSP00000499664.1:n.328-273_328-269dup
ENST00000423557.1:c.445-273_445-269dup MANE Select	ENSP00000412237.1:n.445-273_445-269dup
ENST00000471071.1:n.360-273_360-269dup
NM_000572.2:c.445-273_445-269dup	NP_000563.1:n.445-273_445-269dup
XM_011509506.1:c.445-273_445-269dup	XP_011507808.1:n.445-273_445-269dup
NM_000572.3:c.445-273_445-269dup MANE Select	NP_000563.1:n.445-273_445-269dup
NM_001382624.1:c.190-273_190-269dup	NP_001369553.1:n.190-273_190-269dup
NR_168466.1:n.742-273_742-269dup
NR_168467.1:n.272-273_272-269dup