Canonical Allele Identifier: CA2483126631

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771039G= , CM000663.2:g.206771039G=	GRCh38
NC_000001.10:g.206944384G= , CM000663.1:g.206944384G=	GRCh37
NC_000001.9:g.205011007G=	NCBI36
NG_012088.1:g.6456C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.151C= (IL10)
ENST00000471071.2:c.-10C= (IL10)	ENSP00000493073.2:n.-10C=
ENST00000659065.2:c.129C= (IL10)	ENSP00000499588.1:p.Ala43=
ENST00000659642.2:c.129C= (IL10)	ENSP00000499509.1:p.Ala43=
ENST00000664374.2:c.129C= (IL10)	ENSP00000499664.1:p.Ala43=
ENST00000659997.3:c.-188G= (IL19) MANE Select	ENSP00000499459.2:n.-188G=
ENST00000656872.2:c.-149+209G= (IL19)	ENSP00000499487.2:n.-149+209G=
ENST00000659065.1:c.129C= (IL10)	ENSP00000499588.1:p.Ala43=
ENST00000659642.1:c.129C= (IL10)	ENSP00000499509.1:p.Ala43=
ENST00000659997.2:c.-188G= (IL19)	ENSP00000499459.2:n.-188G=
ENST00000662320.1:n.67+209G= (IL19)
ENST00000664374.1:c.129C= (IL10)	ENSP00000499664.1:p.Ala43=
ENST00000367099.3:n.151C= (IL10)
ENST00000423557.1:c.246C= (IL10) MANE Select	ENSP00000412237.1:p.Ala82=
ENST00000471071.1:n.161C= (IL10)
NM_000572.2:c.246C= (IL10)	NP_000563.1:p.Ala82=
XM_011509506.1:c.246C= (IL10)	XP_011507808.1:p.Ala82=
NM_000572.3:c.246C= (IL10) MANE Select	NP_000563.1:p.Ala82=
NM_153758.3:c.-74G= (IL19)	NP_715639.1:n.-74G=
NM_001382624.1:c.-10C= (IL10)	NP_001369553.1:n.-10C=
NM_001393490.1:c.-149+209G= (IL19)	NP_001380419.1:n.-149+209G=
NM_153758.5:c.-188G= (IL19) MANE Select	NP_715639.2:n.-188G=
NR_168466.1:n.305C= (IL10)