Canonical Allele Identifier: CA1011579453

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1674922528
• gnomAD v3: 1-206773755-C-CCTT
• gnomAD v4: 1-206773755-C-CCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773757_206773759dup , CM000663.2:g.206773757_206773759dup	GRCh38
NC_000001.10:g.206947102_206947104dup , CM000663.1:g.206947102_206947104dup	GRCh37
NC_000001.9:g.205013725_205013727dup	NCBI36
NG_012088.1:g.3737_3739dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.-93_-91dup (IL10)	ENSP00000499588.1:n.-93_-91dup
ENST00000659642.2:c.-1118-322_-1118-320dup (IL10)	ENSP00000499509.1:n.-1118-322_-1118-320du...
ENST00000664374.2:c.-15+572_-15+574dup (IL10)	ENSP00000499664.1:n.-15+572_-15+574dup
ENST00000659997.3:c.-149+2679_-149+2681dup (IL19) MANE Select	ENSP00000499459.2:n.-149+2679_-149+2681du...
ENST00000656872.2:c.-149+2927_-149+2929dup (IL19)	ENSP00000499487.2:n.-149+2927_-149+2929du...
ENST00000659065.1:c.-93_-91dup (IL10)	ENSP00000499588.1:n.-93_-91dup
ENST00000659642.1:c.-1118-322_-1118-320dup (IL10)	ENSP00000499509.1:n.-1118-322_-1118-320du...
ENST00000659997.2:c.-149+2679_-149+2681dup (IL19)	ENSP00000499459.2:n.-149+2679_-149+2681du...
ENST00000662320.1:n.67+2927_67+2929dup (IL19)
ENST00000664374.1:c.-15+572_-15+574dup (IL10)	ENSP00000499664.1:n.-15+572_-15+574dup
XM_011509506.1:c.-1001-322_-1001-320dup (IL10)	XP_011507808.1:n.-1001-322_-1001-320dup
NM_153758.3:c.-35+2679_-35+2681dup (IL19)	NP_715639.1:n.-35+2679_-35+2681dup
NM_001393490.1:c.-149+2927_-149+2929dup (IL19)	NP_001380419.1:n.-149+2927_-149+2929dup
NM_153758.5:c.-149+2679_-149+2681dup (IL19) MANE Select	NP_715639.2:n.-149+2679_-149+2681dup