Canonical Allele Identifier: CA1141675616

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771057A= , CM000663.2:g.206771057A=	GRCh38
NC_000001.10:g.206944402A= , CM000663.1:g.206944402A=	GRCh37
NC_000001.9:g.205011025A=	NCBI36
NG_012088.1:g.6438T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.133T= (IL10)
ENST00000471071.2:c.-28T= (IL10)	ENSP00000493073.2:n.-28T=
ENST00000659065.2:c.111T= (IL10)	ENSP00000499588.1:p.Gly37=
ENST00000659642.2:c.111T= (IL10)	ENSP00000499509.1:p.Gly37=
ENST00000664374.2:c.111T= (IL10)	ENSP00000499664.1:p.Gly37=
ENST00000659997.3:c.-170A= (IL19) MANE Select	ENSP00000499459.2:n.-170A=
ENST00000656872.2:c.-149+227A= (IL19)	ENSP00000499487.2:n.-149+227A=
ENST00000659065.1:c.111T= (IL10)	ENSP00000499588.1:p.Gly37=
ENST00000659642.1:c.111T= (IL10)	ENSP00000499509.1:p.Gly37=
ENST00000659997.2:c.-170A= (IL19)	ENSP00000499459.2:n.-170A=
ENST00000662320.1:n.67+227A= (IL19)
ENST00000664374.1:c.111T= (IL10)	ENSP00000499664.1:p.Gly37=
ENST00000367099.3:n.133T= (IL10)
ENST00000423557.1:c.228T= (IL10) MANE Select	ENSP00000412237.1:p.Gly76=
ENST00000471071.1:n.143T= (IL10)
NM_000572.2:c.228T= (IL10)	NP_000563.1:p.Gly76=
XM_011509506.1:c.228T= (IL10)	XP_011507808.1:p.Gly76=
NM_000572.3:c.228T= (IL10) MANE Select	NP_000563.1:p.Gly76=
NM_153758.3:c.-56A= (IL19)	NP_715639.1:n.-56A=
NM_001382624.1:c.-28T= (IL10)	NP_001369553.1:n.-28T=
NM_001393490.1:c.-149+227A= (IL19)	NP_001380419.1:n.-149+227A=
NM_153758.5:c.-170A= (IL19) MANE Select	NP_715639.2:n.-170A=
NR_168466.1:n.287T= (IL10)