Canonical Allele Identifier: CA2567989318

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773129_206773130insCCCCCTCACCTGAC , CM000663.2:g.206773129_206773130insCCCCCTCACCTGAC	GRCh38
NC_000001.10:g.206946474_206946475insCCCCCTCACCTGAC , CM000663.1:g.206946474_206946475insCCCCCTCACCTGAC	GRCh37
NC_000001.9:g.205013097_205013098insCCCCCTCACCTGAC	NCBI36
NG_012088.1:g.4365_4366insGTCAGGTGAGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-15+550_-15+551insGTCAGGTGAGGGGG (IL10)	ENSP00000499588.1:n.-15+550_-15+551insGTCAGGTGAGGGGG
ENST00000659642.2:c.-812_-811insGTCAGGTGAGGGGG (IL10)	ENSP00000499509.1:n.-812_-811insGTCAGGTGAGGGGG
ENST00000664374.2:c.-14-798_-14-797insGTCAGGTGAGGGGG (IL10)	ENSP00000499664.1:n.-14-798_-14-797insGTCAGGTGAGGGGG
ENST00000659997.3:c.-149+2051_-149+2052insCCCCCTCACCTGAC (IL19) MANE Select	ENSP00000499459.2:n.-149+2051_-149+2052insCCCCCTCACCTGAC
ENST00000656872.2:c.-149+2299_-149+2300insCCCCCTCACCTGAC (IL19)	ENSP00000499487.2:n.-149+2299_-149+2300insCCCCCTCACCTGAC
ENST00000659065.1:c.-15+550_-15+551insGTCAGGTGAGGGGG (IL10)	ENSP00000499588.1:n.-15+550_-15+551insGTCAGGTGAGGGGG
ENST00000659642.1:c.-812_-811insGTCAGGTGAGGGGG (IL10)	ENSP00000499509.1:n.-812_-811insGTCAGGTGAGGGGG
ENST00000659997.2:c.-149+2051_-149+2052insCCCCCTCACCTGAC (IL19)	ENSP00000499459.2:n.-149+2051_-149+2052insCCCCCTCACCTGAC
ENST00000662320.1:n.67+2299_67+2300insCCCCCTCACCTGAC (IL19)
ENST00000664374.1:c.-14-798_-14-797insGTCAGGTGAGGGGG (IL10)	ENSP00000499664.1:n.-14-798_-14-797insGTCAGGTGAGGGGG
XM_011509506.1:c.-695_-694insGTCAGGTGAGGGGG (IL10)	XP_011507808.1:n.-695_-694insGTCAGGTGAGGGGG
NM_153758.3:c.-35+2051_-35+2052insCCCCCTCACCTGAC (IL19)	NP_715639.1:n.-35+2051_-35+2052insCCCCCTCACCTGAC
NM_001393490.1:c.-149+2299_-149+2300insCCCCCTCACCTGAC (IL19)	NP_001380419.1:n.-149+2299_-149+2300insCCCCCTCACCTGAC
NM_153758.5:c.-149+2051_-149+2052insCCCCCTCACCTGAC (IL19) MANE Select	NP_715639.2:n.-149+2051_-149+2052insCCCCCTCACCTGAC