Canonical Allele Identifier: CA730538146

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1188251895
• gnomAD v3: 1-206771295-CAG-C
• gnomAD v4: 1-206771295-CAG-C
• MyVariant Identifiers: chr1:g.206944641_206944642del (hg19) ; chr1:g.206771296_206771297del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771298_206771299del , CM000663.2:g.206771298_206771299del	GRCh38
NC_000001.10:g.206944643_206944644del , CM000663.1:g.206944643_206944644del	GRCh37
NC_000001.9:g.205011266_205011267del	NCBI36
NG_012088.1:g.6198_6199del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.108+59_108+60del (IL10)	ENSP00000499588.1:n.108+59_108+60del
ENST00000659642.2:c.108+59_108+60del (IL10)	ENSP00000499509.1:n.108+59_108+60del
ENST00000664374.2:c.108+59_108+60del (IL10)	ENSP00000499664.1:n.108+59_108+60del
ENST00000659997.3:c.-149+220_-149+221del (IL19) MANE Select	ENSP00000499459.2:n.-149+220_-149+221del
ENST00000656872.2:c.-149+468_-149+469del (IL19)	ENSP00000499487.2:n.-149+468_-149+469del
ENST00000659065.1:c.108+59_108+60del (IL10)	ENSP00000499588.1:n.108+59_108+60del
ENST00000659642.1:c.108+59_108+60del (IL10)	ENSP00000499509.1:n.108+59_108+60del
ENST00000659997.2:c.-149+220_-149+221del (IL19)	ENSP00000499459.2:n.-149+220_-149+221del
ENST00000662320.1:n.67+468_67+469del (IL19)
ENST00000664374.1:c.108+59_108+60del (IL10)	ENSP00000499664.1:n.108+59_108+60del
ENST00000423557.1:c.225+59_225+60del (IL10) MANE Select	ENSP00000412237.1:n.225+59_225+60del
NM_000572.2:c.225+59_225+60del (IL10)	NP_000563.1:n.225+59_225+60del
XM_011509506.1:c.225+59_225+60del (IL10)	XP_011507808.1:n.225+59_225+60del
NM_000572.3:c.225+59_225+60del (IL10) MANE Select	NP_000563.1:n.225+59_225+60del
NM_153758.3:c.-35+220_-35+221del (IL19)	NP_715639.1:n.-35+220_-35+221del
NM_001393490.1:c.-149+468_-149+469del (IL19)	NP_001380419.1:n.-149+468_-149+469del
NM_153758.5:c.-149+220_-149+221del (IL19) MANE Select	NP_715639.2:n.-149+220_-149+221del
NR_168466.1:n.284+59_284+60del (IL10)