Canonical Allele Identifier: CA2483126617

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770995_206770996delinsTG , CM000663.2:g.206770995_206770996delinsTG	GRCh38
NC_000001.10:g.206944340_206944341delinsTG , CM000663.1:g.206944340_206944341delinsTG	GRCh37
NC_000001.9:g.205010963_205010964delinsTG	NCBI36
NG_012088.1:g.6499_6500delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.194_195delinsCA (IL10)
ENST00000471071.2:c.34_35delinsCA (IL10)	ENSP00000493073.2:p.Gln12=
ENST00000659065.2:c.172_173delinsCA (IL10)	ENSP00000499588.1:p.Gln58=
ENST00000659642.2:c.172_173delinsCA (IL10)	ENSP00000499509.1:p.Gln58=
ENST00000664374.2:c.172_173delinsCA (IL10)	ENSP00000499664.1:p.Gln58=
ENST00000659997.3:c.-232_-231delinsTG (IL19) MANE Select	ENSP00000499459.2:n.-232_-231delinsTG
ENST00000656872.2:c.-149+165_-149+166delinsTG (IL19)	ENSP00000499487.2:n.-149+165_-149+166delinsTG
ENST00000659065.1:c.172_173delinsCA (IL10)	ENSP00000499588.1:p.Gln58=
ENST00000659642.1:c.172_173delinsCA (IL10)	ENSP00000499509.1:p.Gln58=
ENST00000659997.2:c.-232_-231delinsTG (IL19)	ENSP00000499459.2:n.-232_-231delinsTG
ENST00000662320.1:n.67+165_67+166delinsTG (IL19)
ENST00000664374.1:c.172_173delinsCA (IL10)	ENSP00000499664.1:p.Gln58=
ENST00000367099.3:n.194_195delinsCA (IL10)
ENST00000423557.1:c.289_290delinsCA (IL10) MANE Select	ENSP00000412237.1:p.Gln97=
ENST00000471071.1:n.204_205delinsCA (IL10)
NM_000572.2:c.289_290delinsCA (IL10)	NP_000563.1:p.Gln97=
XM_011509506.1:c.289_290delinsCA (IL10)	XP_011507808.1:p.Gln97=
NM_000572.3:c.289_290delinsCA (IL10) MANE Select	NP_000563.1:p.Gln97=
NM_153758.3:c.-118_-117delinsTG (IL19)	NP_715639.1:n.-118_-117delinsTG
NM_001382624.1:c.34_35delinsCA (IL10)	NP_001369553.1:p.Gln12=
NM_001393490.1:c.-149+165_-149+166delinsTG (IL19)	NP_001380419.1:n.-149+165_-149+166delinsTG
NM_153758.5:c.-232_-231delinsTG (IL19) MANE Select	NP_715639.2:n.-232_-231delinsTG
NR_168466.1:n.348_349delinsCA (IL10)