Canonical Allele Identifier: CA2483126624

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771024G= , CM000663.2:g.206771024G=	GRCh38
NC_000001.10:g.206944369G= , CM000663.1:g.206944369G=	GRCh37
NC_000001.9:g.205010992G=	NCBI36
NG_012088.1:g.6471C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.166C= (IL10)
ENST00000471071.2:c.6C= (IL10)	ENSP00000493073.2:p.Ile2=
ENST00000659065.2:c.144C= (IL10)	ENSP00000499588.1:p.Ile48=
ENST00000659642.2:c.144C= (IL10)	ENSP00000499509.1:p.Ile48=
ENST00000664374.2:c.144C= (IL10)	ENSP00000499664.1:p.Ile48=
ENST00000659997.3:c.-203G= (IL19) MANE Select	ENSP00000499459.2:n.-203G=
ENST00000656872.2:c.-149+194G= (IL19)	ENSP00000499487.2:n.-149+194G=
ENST00000659065.1:c.144C= (IL10)	ENSP00000499588.1:p.Ile48=
ENST00000659642.1:c.144C= (IL10)	ENSP00000499509.1:p.Ile48=
ENST00000659997.2:c.-203G= (IL19)	ENSP00000499459.2:n.-203G=
ENST00000662320.1:n.67+194G= (IL19)
ENST00000664374.1:c.144C= (IL10)	ENSP00000499664.1:p.Ile48=
ENST00000367099.3:n.166C= (IL10)
ENST00000423557.1:c.261C= (IL10) MANE Select	ENSP00000412237.1:p.Ile87=
ENST00000471071.1:n.176C= (IL10)
NM_000572.2:c.261C= (IL10)	NP_000563.1:p.Ile87=
XM_011509506.1:c.261C= (IL10)	XP_011507808.1:p.Ile87=
NM_000572.3:c.261C= (IL10) MANE Select	NP_000563.1:p.Ile87=
NM_153758.3:c.-89G= (IL19)	NP_715639.1:n.-89G=
NM_001382624.1:c.6C= (IL10)	NP_001369553.1:p.Ile2=
NM_001393490.1:c.-149+194G= (IL19)	NP_001380419.1:n.-149+194G=
NM_153758.5:c.-203G= (IL19) MANE Select	NP_715639.2:n.-203G=
NR_168466.1:n.320C= (IL10)