Canonical Allele Identifier: CA2483126935

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771843_206771844delinsGT , CM000663.2:g.206771843_206771844delinsGT	GRCh38
NC_000001.10:g.206945188_206945189delinsGT , CM000663.1:g.206945188_206945189delinsGT	GRCh37
NC_000001.9:g.205011811_205011812delinsGT	NCBI36
NG_012088.1:g.5651_5652delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.48+427_49-428delinsAC (IL10)	ENSP00000499588.1:n.48+427_49-428delinsAC
ENST00000659642.2:c.48+427_49-428delinsAC (IL10)	ENSP00000499509.1:n.48+427_49-428delinsAC
ENST00000664374.2:c.48+427_49-428delinsAC (IL10)	ENSP00000499664.1:n.48+427_49-428delinsAC
ENST00000659997.3:c.-149+765_-149+766delinsGT (IL19) MANE Select	ENSP00000499459.2:n.-149+765_-149+766delinsGT
ENST00000656872.2:c.-149+1013_-149+1014delinsGT (IL19)	ENSP00000499487.2:n.-149+1013_-149+1014delinsGT
ENST00000659065.1:c.48+427_49-428delinsAC (IL10)	ENSP00000499588.1:n.48+427_49-428delinsAC
ENST00000659642.1:c.48+427_49-428delinsAC (IL10)	ENSP00000499509.1:n.48+427_49-428delinsAC
ENST00000659997.2:c.-149+765_-149+766delinsGT (IL19)	ENSP00000499459.2:n.-149+765_-149+766delinsGT
ENST00000662320.1:n.67+1013_67+1014delinsGT (IL19)
ENST00000664374.1:c.48+427_49-428delinsAC (IL10)	ENSP00000499664.1:n.48+427_49-428delinsAC
ENST00000423557.1:c.165+427_166-428delinsAC (IL10) MANE Select	ENSP00000412237.1:n.165+427_166-428delinsAC
NM_000572.2:c.165+427_166-428delinsAC (IL10)	NP_000563.1:n.165+427_166-428delinsAC
XM_011509506.1:c.165+427_166-428delinsAC (IL10)	XP_011507808.1:n.165+427_166-428delinsAC
NM_000572.3:c.165+427_166-428delinsAC (IL10) MANE Select	NP_000563.1:n.165+427_166-428delinsAC
NM_153758.3:c.-35+765_-35+766delinsGT (IL19)	NP_715639.1:n.-35+765_-35+766delinsGT
NM_001393490.1:c.-149+1013_-149+1014delinsGT (IL19)	NP_001380419.1:n.-149+1013_-149+1014delinsGT
NM_153758.5:c.-149+765_-149+766delinsGT (IL19) MANE Select	NP_715639.2:n.-149+765_-149+766delinsGT
NR_168466.1:n.224+427_225-428delinsAC (IL10)