Canonical Allele Identifier: CA2697953284

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs2102440601

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206772042_206772070dup , CM000663.2:g.206772042_206772070dup	GRCh38
NC_000001.10:g.206945387_206945415dup , CM000663.1:g.206945387_206945415dup	GRCh37
NC_000001.9:g.205012010_205012038dup	NCBI36
NG_012088.1:g.5426_5454dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.48+202_48+230dup (IL10)	ENSP00000499588.1:n.48+202_48+230dup
ENST00000659642.2:c.48+202_48+230dup (IL10)	ENSP00000499509.1:n.48+202_48+230dup
ENST00000664374.2:c.48+202_48+230dup (IL10)	ENSP00000499664.1:n.48+202_48+230dup
ENST00000659997.3:c.-149+964_-149+992dup (IL19) MANE Select	ENSP00000499459.2:n.-149+964_-149+992dup
ENST00000656872.2:c.-149+1212_-149+1240dup (IL19)	ENSP00000499487.2:n.-149+1212_-149+1240du...
ENST00000659065.1:c.48+202_48+230dup (IL10)	ENSP00000499588.1:n.48+202_48+230dup
ENST00000659642.1:c.48+202_48+230dup (IL10)	ENSP00000499509.1:n.48+202_48+230dup
ENST00000659997.2:c.-149+964_-149+992dup (IL19)	ENSP00000499459.2:n.-149+964_-149+992dup
ENST00000662320.1:n.67+1212_67+1240dup (IL19)
ENST00000664374.1:c.48+202_48+230dup (IL10)	ENSP00000499664.1:n.48+202_48+230dup
ENST00000423557.1:c.165+202_165+230dup (IL10) MANE Select	ENSP00000412237.1:n.165+202_165+230dup
NM_000572.2:c.165+202_165+230dup (IL10)	NP_000563.1:n.165+202_165+230dup
XM_011509506.1:c.165+202_165+230dup (IL10)	XP_011507808.1:n.165+202_165+230dup
NM_000572.3:c.165+202_165+230dup (IL10) MANE Select	NP_000563.1:n.165+202_165+230dup
NM_153758.3:c.-35+964_-35+992dup (IL19)	NP_715639.1:n.-35+964_-35+992dup
NM_001393490.1:c.-149+1212_-149+1240dup (IL19)	NP_001380419.1:n.-149+1212_-149+1240dup
NM_153758.5:c.-149+964_-149+992dup (IL19) MANE Select	NP_715639.2:n.-149+964_-149+992dup
NR_168466.1:n.224+202_224+230dup (IL10)