Canonical Allele Identifier: CA646375361

Gene: IL10 IL19

Linked Data

• COSMIC: COSN25442657

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771979_206771990del , CM000663.2:g.206771979_206771990del	GRCh38
NC_000001.10:g.206945324_206945335del , CM000663.1:g.206945324_206945335del	GRCh37
NC_000001.9:g.205011947_205011958del	NCBI36
NG_012088.1:g.5505_5516del

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.48+281_48+292del (IL10)	ENSP00000499588.1:n.48+281_48+292del
ENST00000659642.2:c.48+281_48+292del (IL10)	ENSP00000499509.1:n.48+281_48+292del
ENST00000664374.2:c.48+281_48+292del (IL10)	ENSP00000499664.1:n.48+281_48+292del
ENST00000659997.3:c.-149+901_-149+912del (IL19) MANE Select	ENSP00000499459.2:n.-149+901_-149+912del
ENST00000656872.2:c.-149+1149_-149+1160del (IL19)	ENSP00000499487.2:n.-149+1149_-149+1160de...
ENST00000659065.1:c.48+281_48+292del (IL10)	ENSP00000499588.1:n.48+281_48+292del
ENST00000659642.1:c.48+281_48+292del (IL10)	ENSP00000499509.1:n.48+281_48+292del
ENST00000659997.2:c.-149+901_-149+912del (IL19)	ENSP00000499459.2:n.-149+901_-149+912del
ENST00000662320.1:n.67+1149_67+1160del (IL19)
ENST00000664374.1:c.48+281_48+292del (IL10)	ENSP00000499664.1:n.48+281_48+292del
ENST00000423557.1:c.165+281_165+292del (IL10) MANE Select	ENSP00000412237.1:n.165+281_165+292del
NM_000572.2:c.165+281_165+292del (IL10)	NP_000563.1:n.165+281_165+292del
XM_011509506.1:c.165+281_165+292del (IL10)	XP_011507808.1:n.165+281_165+292del
NM_000572.3:c.165+281_165+292del (IL10) MANE Select	NP_000563.1:n.165+281_165+292del
NM_153758.3:c.-35+901_-35+912del (IL19)	NP_715639.1:n.-35+901_-35+912del
NM_001393490.1:c.-149+1149_-149+1160del (IL19)	NP_001380419.1:n.-149+1149_-149+1160del
NM_153758.5:c.-149+901_-149+912del (IL19) MANE Select	NP_715639.2:n.-149+901_-149+912del
NR_168466.1:n.224+281_224+292del (IL10)