Canonical Allele Identifier: CA2483127488

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773081T= , CM000663.2:g.206773081T=	GRCh38
NC_000001.10:g.206946426T= , CM000663.1:g.206946426T=	GRCh37
NC_000001.9:g.205013049T=	NCBI36
NG_012088.1:g.4414A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-15+599A= (IL10)	ENSP00000499588.1:n.-15+599A=
ENST00000659642.2:c.-763A= (IL10)	ENSP00000499509.1:n.-763A=
ENST00000664374.2:c.-14-749A= (IL10)	ENSP00000499664.1:n.-14-749A=
ENST00000659997.3:c.-149+2003T= (IL19) MANE Select	ENSP00000499459.2:n.-149+2003T=
ENST00000656872.2:c.-149+2251T= (IL19)	ENSP00000499487.2:n.-149+2251T=
ENST00000659065.1:c.-15+599A= (IL10)	ENSP00000499588.1:n.-15+599A=
ENST00000659642.1:c.-763A= (IL10)	ENSP00000499509.1:n.-763A=
ENST00000659997.2:c.-149+2003T= (IL19)	ENSP00000499459.2:n.-149+2003T=
ENST00000662320.1:n.67+2251T= (IL19)
ENST00000664374.1:c.-14-749A= (IL10)	ENSP00000499664.1:n.-14-749A=
XM_011509506.1:c.-646A= (IL10)	XP_011507808.1:n.-646A=
NM_153758.3:c.-35+2003T= (IL19)	NP_715639.1:n.-35+2003T=
NM_001393490.1:c.-149+2251T= (IL19)	NP_001380419.1:n.-149+2251T=
NM_153758.5:c.-149+2003T= (IL19) MANE Select	NP_715639.2:n.-149+2003T=