Canonical Allele Identifier: CA2747495656

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771534_206771539dup , CM000663.2:g.206771534_206771539dup	GRCh38
NC_000001.10:g.206944879_206944884dup , CM000663.1:g.206944879_206944884dup	GRCh37
NC_000001.9:g.205011502_205011507dup	NCBI36
NG_012088.1:g.5957_5962dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.49-123_49-118dup (IL10)	ENSP00000499588.1:n.49-123_49-118dup
ENST00000659642.2:c.49-123_49-118dup (IL10)	ENSP00000499509.1:n.49-123_49-118dup
ENST00000664374.2:c.49-123_49-118dup (IL10)	ENSP00000499664.1:n.49-123_49-118dup
ENST00000659997.3:c.-149+456_-149+461dup (IL19) MANE Select	ENSP00000499459.2:n.-149+456_-149+461dup
ENST00000656872.2:c.-149+704_-149+709dup (IL19)	ENSP00000499487.2:n.-149+704_-149+709dup
ENST00000659065.1:c.49-123_49-118dup (IL10)	ENSP00000499588.1:n.49-123_49-118dup
ENST00000659642.1:c.49-123_49-118dup (IL10)	ENSP00000499509.1:n.49-123_49-118dup
ENST00000659997.2:c.-149+456_-149+461dup (IL19)	ENSP00000499459.2:n.-149+456_-149+461dup
ENST00000662320.1:n.67+704_67+709dup (IL19)
ENST00000664374.1:c.49-123_49-118dup (IL10)	ENSP00000499664.1:n.49-123_49-118dup
ENST00000423557.1:c.166-123_166-118dup (IL10) MANE Select	ENSP00000412237.1:n.166-123_166-118dup
NM_000572.2:c.166-123_166-118dup (IL10)	NP_000563.1:n.166-123_166-118dup
XM_011509506.1:c.166-123_166-118dup (IL10)	XP_011507808.1:n.166-123_166-118dup
NM_000572.3:c.166-123_166-118dup (IL10) MANE Select	NP_000563.1:n.166-123_166-118dup
NM_153758.3:c.-35+456_-35+461dup (IL19)	NP_715639.1:n.-35+456_-35+461dup
NM_001393490.1:c.-149+704_-149+709dup (IL19)	NP_001380419.1:n.-149+704_-149+709dup
NM_153758.5:c.-149+456_-149+461dup (IL19) MANE Select	NP_715639.2:n.-149+456_-149+461dup
NR_168466.1:n.225-123_225-118dup (IL10)