Canonical Allele Identifier: CA2483126984

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771952_206771953delinsAC , CM000663.2:g.206771952_206771953delinsAC	GRCh38
NC_000001.10:g.206945297_206945298delinsAC , CM000663.1:g.206945297_206945298delinsAC	GRCh37
NC_000001.9:g.205011920_205011921delinsAC	NCBI36
NG_012088.1:g.5542_5543delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.48+318_48+319delinsGT (IL10)	ENSP00000499588.1:n.48+318_48+319delinsGT
ENST00000659642.2:c.48+318_48+319delinsGT (IL10)	ENSP00000499509.1:n.48+318_48+319delinsGT
ENST00000664374.2:c.48+318_48+319delinsGT (IL10)	ENSP00000499664.1:n.48+318_48+319delinsGT
ENST00000659997.3:c.-149+874_-149+875delinsAC (IL19) MANE Select	ENSP00000499459.2:n.-149+874_-149+875delinsAC
ENST00000656872.2:c.-149+1122_-149+1123delinsAC (IL19)	ENSP00000499487.2:n.-149+1122_-149+1123delinsAC
ENST00000659065.1:c.48+318_48+319delinsGT (IL10)	ENSP00000499588.1:n.48+318_48+319delinsGT
ENST00000659642.1:c.48+318_48+319delinsGT (IL10)	ENSP00000499509.1:n.48+318_48+319delinsGT
ENST00000659997.2:c.-149+874_-149+875delinsAC (IL19)	ENSP00000499459.2:n.-149+874_-149+875delinsAC
ENST00000662320.1:n.67+1122_67+1123delinsAC (IL19)
ENST00000664374.1:c.48+318_48+319delinsGT (IL10)	ENSP00000499664.1:n.48+318_48+319delinsGT
ENST00000423557.1:c.165+318_165+319delinsGT (IL10) MANE Select	ENSP00000412237.1:n.165+318_165+319delinsGT
NM_000572.2:c.165+318_165+319delinsGT (IL10)	NP_000563.1:n.165+318_165+319delinsGT
XM_011509506.1:c.165+318_165+319delinsGT (IL10)	XP_011507808.1:n.165+318_165+319delinsGT
NM_000572.3:c.165+318_165+319delinsGT (IL10) MANE Select	NP_000563.1:n.165+318_165+319delinsGT
NM_153758.3:c.-35+874_-35+875delinsAC (IL19)	NP_715639.1:n.-35+874_-35+875delinsAC
NM_001393490.1:c.-149+1122_-149+1123delinsAC (IL19)	NP_001380419.1:n.-149+1122_-149+1123delinsAC
NM_153758.5:c.-149+874_-149+875delinsAC (IL19) MANE Select	NP_715639.2:n.-149+874_-149+875delinsAC
NR_168466.1:n.224+318_224+319delinsGT (IL10)