Canonical Allele Identifier: CA2483127443

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206772987_206772988delinsAG , CM000663.2:g.206772987_206772988delinsAG	GRCh38
NC_000001.10:g.206946332_206946333delinsAG , CM000663.1:g.206946332_206946333delinsAG	GRCh37
NC_000001.9:g.205012955_205012956delinsAG	NCBI36
NG_012088.1:g.4507_4508delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-14-656_-14-655delinsCT (IL10)	ENSP00000499588.1:n.-14-656_-14-655delinsCT
ENST00000659642.2:c.-670_-669delinsCT (IL10)	ENSP00000499509.1:n.-670_-669delinsCT
ENST00000664374.2:c.-14-656_-14-655delinsCT (IL10)	ENSP00000499664.1:n.-14-656_-14-655delinsCT
ENST00000659997.3:c.-149+1909_-149+1910delinsAG (IL19) MANE Select	ENSP00000499459.2:n.-149+1909_-149+1910delinsAG
ENST00000656872.2:c.-149+2157_-149+2158delinsAG (IL19)	ENSP00000499487.2:n.-149+2157_-149+2158delinsAG
ENST00000659065.1:c.-14-656_-14-655delinsCT (IL10)	ENSP00000499588.1:n.-14-656_-14-655delinsCT
ENST00000659642.1:c.-670_-669delinsCT (IL10)	ENSP00000499509.1:n.-670_-669delinsCT
ENST00000659997.2:c.-149+1909_-149+1910delinsAG (IL19)	ENSP00000499459.2:n.-149+1909_-149+1910delinsAG
ENST00000662320.1:n.67+2157_67+2158delinsAG (IL19)
ENST00000664374.1:c.-14-656_-14-655delinsCT (IL10)	ENSP00000499664.1:n.-14-656_-14-655delinsCT
XM_011509506.1:c.-553_-552delinsCT (IL10)	XP_011507808.1:n.-553_-552delinsCT
NM_153758.3:c.-35+1909_-35+1910delinsAG (IL19)	NP_715639.1:n.-35+1909_-35+1910delinsAG
NM_001393490.1:c.-149+2157_-149+2158delinsAG (IL19)	NP_001380419.1:n.-149+2157_-149+2158delinsAG
NM_153758.5:c.-149+1909_-149+1910delinsAG (IL19) MANE Select	NP_715639.2:n.-149+1909_-149+1910delinsAG