Canonical Allele Identifier: CA1011578922

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1674901462
• gnomAD v3: 1-206773112-TA-T
• gnomAD v4: 1-206773112-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773113del , CM000663.2:g.206773113del	GRCh38
NC_000001.10:g.206946458del , CM000663.1:g.206946458del	GRCh37
NC_000001.9:g.205013081del	NCBI36
NG_012088.1:g.4382del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-15+567del (IL10)	ENSP00000499588.1:n.-15+567del
ENST00000659642.2:c.-795del (IL10)	ENSP00000499509.1:n.-795del
ENST00000664374.2:c.-14-781del (IL10)	ENSP00000499664.1:n.-14-781del
ENST00000659997.3:c.-149+2035del (IL19) MANE Select	ENSP00000499459.2:n.-149+2035del
ENST00000656872.2:c.-149+2283del (IL19)	ENSP00000499487.2:n.-149+2283del
ENST00000659065.1:c.-15+567del (IL10)	ENSP00000499588.1:n.-15+567del
ENST00000659642.1:c.-795del (IL10)	ENSP00000499509.1:n.-795del
ENST00000659997.2:c.-149+2035del (IL19)	ENSP00000499459.2:n.-149+2035del
ENST00000662320.1:n.67+2283del (IL19)
ENST00000664374.1:c.-14-781del (IL10)	ENSP00000499664.1:n.-14-781del
XM_011509506.1:c.-678del (IL10)	XP_011507808.1:n.-678del
NM_153758.3:c.-35+2035del (IL19)	NP_715639.1:n.-35+2035del
NM_001393490.1:c.-149+2283del (IL19)	NP_001380419.1:n.-149+2283del
NM_153758.5:c.-149+2035del (IL19) MANE Select	NP_715639.2:n.-149+2035del