Canonical Allele Identifier: CA1363759

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs753066499
• ExAC: 1:206944229 G / GA
• gnomAD v2: 1-206944229-G-GA
• gnomAD v3: 1-206770884-G-GA
• gnomAD v4: 1-206770884-G-GA
• MyVariant Identifiers: chr1:g.206944229_206944230insA (hg19) ; chr1:g.206770884_206770885insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770890dup , CM000663.2:g.206770890dup	GRCh38
NC_000001.10:g.206944235dup , CM000663.1:g.206944235dup	GRCh37
NC_000001.9:g.205010858dup	NCBI36
NG_012088.1:g.6610dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.283+22dup (IL10)
ENST00000471071.2:c.123+22dup (IL10)	ENSP00000493073.2:n.123+22dup
ENST00000659065.2:c.261+22dup (IL10)	ENSP00000499588.1:n.261+22dup
ENST00000659642.2:c.261+22dup (IL10)	ENSP00000499509.1:n.261+22dup
ENST00000664374.2:c.261+22dup (IL10)	ENSP00000499664.1:n.261+22dup
ENST00000659997.3:c.-337dup (IL19) MANE Select	ENSP00000499459.2:n.-337dup
ENST00000656872.2:c.-149+60dup (IL19)	ENSP00000499487.2:n.-149+60dup
ENST00000659065.1:c.261+22dup (IL10)	ENSP00000499588.1:n.261+22dup
ENST00000659642.1:c.261+22dup (IL10)	ENSP00000499509.1:n.261+22dup
ENST00000659997.2:c.-337dup (IL19)	ENSP00000499459.2:n.-337dup
ENST00000662320.1:n.67+60dup (IL19)
ENST00000664374.1:c.261+22dup (IL10)	ENSP00000499664.1:n.261+22dup
ENST00000367099.3:n.283+22dup (IL10)
ENST00000423557.1:c.378+22dup (IL10) MANE Select	ENSP00000412237.1:n.378+22dup
ENST00000471071.1:n.293+22dup (IL10)
NM_000572.2:c.378+22dup (IL10)	NP_000563.1:n.378+22dup
XM_011509506.1:c.378+22dup (IL10)	XP_011507808.1:n.378+22dup
NM_000572.3:c.378+22dup (IL10) MANE Select	NP_000563.1:n.378+22dup
NM_153758.3:c.-223dup (IL19)	NP_715639.1:n.-223dup
NM_001382624.1:c.123+22dup (IL10)	NP_001369553.1:n.123+22dup
NM_001393490.1:c.-149+60dup (IL19)	NP_001380419.1:n.-149+60dup
NM_153758.5:c.-337dup (IL19) MANE Select	NP_715639.2:n.-337dup
NR_168466.1:n.437+22dup (IL10)