Canonical Allele Identifier: CA2483126652

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771098A= , CM000663.2:g.206771098A=	GRCh38
NC_000001.10:g.206944443A= , CM000663.1:g.206944443A=	GRCh37
NC_000001.9:g.205011066A=	NCBI36
NG_012088.1:g.6397T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.92T= (IL10)
ENST00000471071.2:c.-69T= (IL10)	ENSP00000493073.2:n.-69T=
ENST00000659065.2:c.109-39T= (IL10)	ENSP00000499588.1:n.109-39T=
ENST00000659642.2:c.109-39T= (IL10)	ENSP00000499509.1:n.109-39T=
ENST00000664374.2:c.109-39T= (IL10)	ENSP00000499664.1:n.109-39T=
ENST00000659997.3:c.-149+20A= (IL19) MANE Select	ENSP00000499459.2:n.-149+20A=
ENST00000656872.2:c.-149+268A= (IL19)	ENSP00000499487.2:n.-149+268A=
ENST00000659065.1:c.109-39T= (IL10)	ENSP00000499588.1:n.109-39T=
ENST00000659642.1:c.109-39T= (IL10)	ENSP00000499509.1:n.109-39T=
ENST00000659997.2:c.-149+20A= (IL19)	ENSP00000499459.2:n.-149+20A=
ENST00000662320.1:n.67+268A= (IL19)
ENST00000664374.1:c.109-39T= (IL10)	ENSP00000499664.1:n.109-39T=
ENST00000367099.3:n.92T= (IL10)
ENST00000423557.1:c.226-39T= (IL10) MANE Select	ENSP00000412237.1:n.226-39T=
ENST00000471071.1:n.102T= (IL10)
NM_000572.2:c.226-39T= (IL10)	NP_000563.1:n.226-39T=
XM_011509506.1:c.226-39T= (IL10)	XP_011507808.1:n.226-39T=
NM_000572.3:c.226-39T= (IL10) MANE Select	NP_000563.1:n.226-39T=
NM_153758.3:c.-35+20A= (IL19)	NP_715639.1:n.-35+20A=
NM_001382624.1:c.-69T= (IL10)	NP_001369553.1:n.-69T=
NM_001393490.1:c.-149+268A= (IL19)	NP_001380419.1:n.-149+268A=
NM_153758.5:c.-149+20A= (IL19) MANE Select	NP_715639.2:n.-149+20A=
NR_168466.1:n.285-39T= (IL10)