Canonical Allele Identifier: CA2483127425

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206772958_206772960delinsCTG , CM000663.2:g.206772958_206772960delinsCTG	GRCh38
NC_000001.10:g.206946303_206946305delinsCTG , CM000663.1:g.206946303_206946305delinsCTG	GRCh37
NC_000001.9:g.205012926_205012928delinsCTG	NCBI36
NG_012088.1:g.4535_4537delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-14-628_-14-626delinsCAG (IL10)	ENSP00000499588.1:n.-14-628_-14-626delinsCAG
ENST00000659642.2:c.-642_-640delinsCAG (IL10)	ENSP00000499509.1:n.-642_-640delinsCAG
ENST00000664374.2:c.-14-628_-14-626delinsCAG (IL10)	ENSP00000499664.1:n.-14-628_-14-626delinsCAG
ENST00000659997.3:c.-149+1880_-149+1882delinsCTG (IL19) MANE Select	ENSP00000499459.2:n.-149+1880_-149+1882delinsCTG
ENST00000656872.2:c.-149+2128_-149+2130delinsCTG (IL19)	ENSP00000499487.2:n.-149+2128_-149+2130delinsCTG
ENST00000659065.1:c.-14-628_-14-626delinsCAG (IL10)	ENSP00000499588.1:n.-14-628_-14-626delinsCAG
ENST00000659642.1:c.-642_-640delinsCAG (IL10)	ENSP00000499509.1:n.-642_-640delinsCAG
ENST00000659997.2:c.-149+1880_-149+1882delinsCTG (IL19)	ENSP00000499459.2:n.-149+1880_-149+1882delinsCTG
ENST00000662320.1:n.67+2128_67+2130delinsCTG (IL19)
ENST00000664374.1:c.-14-628_-14-626delinsCAG (IL10)	ENSP00000499664.1:n.-14-628_-14-626delinsCAG
XM_011509506.1:c.-525_-523delinsCAG (IL10)	XP_011507808.1:n.-525_-523delinsCAG
NM_153758.3:c.-35+1880_-35+1882delinsCTG (IL19)	NP_715639.1:n.-35+1880_-35+1882delinsCTG
NM_001393490.1:c.-149+2128_-149+2130delinsCTG (IL19)	NP_001380419.1:n.-149+2128_-149+2130delinsCTG
NM_153758.5:c.-149+1880_-149+1882delinsCTG (IL19) MANE Select	NP_715639.2:n.-149+1880_-149+1882delinsCTG