Canonical Allele Identifier: CA2483127418

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206772949C= , CM000663.2:g.206772949C=	GRCh38
NC_000001.10:g.206946294C= , CM000663.1:g.206946294C=	GRCh37
NC_000001.9:g.205012917C=	NCBI36
NG_012088.1:g.4546G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-14-617G= (IL10)	ENSP00000499588.1:n.-14-617G=
ENST00000659642.2:c.-631G= (IL10)	ENSP00000499509.1:n.-631G=
ENST00000664374.2:c.-14-617G= (IL10)	ENSP00000499664.1:n.-14-617G=
ENST00000659997.3:c.-149+1871C= (IL19) MANE Select	ENSP00000499459.2:n.-149+1871C=
ENST00000656872.2:c.-149+2119C= (IL19)	ENSP00000499487.2:n.-149+2119C=
ENST00000659065.1:c.-14-617G= (IL10)	ENSP00000499588.1:n.-14-617G=
ENST00000659642.1:c.-631G= (IL10)	ENSP00000499509.1:n.-631G=
ENST00000659997.2:c.-149+1871C= (IL19)	ENSP00000499459.2:n.-149+1871C=
ENST00000662320.1:n.67+2119C= (IL19)
ENST00000664374.1:c.-14-617G= (IL10)	ENSP00000499664.1:n.-14-617G=
XM_011509506.1:c.-514G= (IL10)	XP_011507808.1:n.-514G=
NM_153758.3:c.-35+1871C= (IL19)	NP_715639.1:n.-35+1871C=
NM_001393490.1:c.-149+2119C= (IL19)	NP_001380419.1:n.-149+2119C=
NM_153758.5:c.-149+1871C= (IL19) MANE Select	NP_715639.2:n.-149+1871C=