Canonical Allele Identifier: CA1011592563

Gene: IL10

Linked Data

• dbSNP Id: rs1673510500
• gnomAD v3: 1-206769016-AT-A
• gnomAD v4: 1-206769016-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206769018del , CM000663.2:g.206769018del	GRCh38
NC_000001.10:g.206942363del , CM000663.1:g.206942363del	GRCh37
NC_000001.9:g.205008986del	NCBI36
NG_012088.1:g.8478del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.1161del
ENST00000471071.2:c.190-289del	ENSP00000493073.2:n.190-289del
ENST00000640756.2:n.255-289del
ENST00000659065.2:c.328-289del	ENSP00000499588.1:n.328-289del
ENST00000659642.2:c.328-289del	ENSP00000499509.1:n.328-289del
ENST00000664374.2:c.328-289del	ENSP00000499664.1:n.328-289del
ENST00000640756.1:n.244-289del
ENST00000659065.1:c.328-289del	ENSP00000499588.1:n.328-289del
ENST00000659642.1:c.328-289del	ENSP00000499509.1:n.328-289del
ENST00000664374.1:c.328-289del	ENSP00000499664.1:n.328-289del
ENST00000423557.1:c.445-289del MANE Select	ENSP00000412237.1:n.445-289del
ENST00000471071.1:n.360-289del
NM_000572.2:c.445-289del	NP_000563.1:n.445-289del
XM_011509506.1:c.445-289del	XP_011507808.1:n.445-289del
NM_000572.3:c.445-289del MANE Select	NP_000563.1:n.445-289del
NM_001382624.1:c.190-289del	NP_001369553.1:n.190-289del
NR_168466.1:n.742-289del
NR_168467.1:n.272-289del