Canonical Allele Identifier: CA528574920

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1460504582
• gnomAD v2: 1-206946332-AGGGGGT-A
• gnomAD v3: 1-206772987-AGGGGGT-A
• gnomAD v4: 1-206772987-AGGGGGT-A
• MyVariant Identifiers: chr1:g.206946333_206946338del (hg19) ; chr1:g.206772988_206772993del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206772991_206772996del , CM000663.2:g.206772991_206772996del	GRCh38
NC_000001.10:g.206946336_206946341del , CM000663.1:g.206946336_206946341del	GRCh37
NC_000001.9:g.205012959_205012964del	NCBI36
NG_012088.1:g.4502_4507del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-14-661_-14-656del (IL10)	ENSP00000499588.1:n.-14-661_-14-656del
ENST00000659642.2:c.-675_-670del (IL10)	ENSP00000499509.1:n.-675_-670del
ENST00000664374.2:c.-14-661_-14-656del (IL10)	ENSP00000499664.1:n.-14-661_-14-656del
ENST00000659997.3:c.-149+1913_-149+1918del (IL19) MANE Select	ENSP00000499459.2:n.-149+1913_-149+1918del
ENST00000656872.2:c.-149+2161_-149+2166del (IL19)	ENSP00000499487.2:n.-149+2161_-149+2166del
ENST00000659065.1:c.-14-661_-14-656del (IL10)	ENSP00000499588.1:n.-14-661_-14-656del
ENST00000659642.1:c.-675_-670del (IL10)	ENSP00000499509.1:n.-675_-670del
ENST00000659997.2:c.-149+1913_-149+1918del (IL19)	ENSP00000499459.2:n.-149+1913_-149+1918del
ENST00000662320.1:n.67+2161_67+2166del (IL19)
ENST00000664374.1:c.-14-661_-14-656del (IL10)	ENSP00000499664.1:n.-14-661_-14-656del
XM_011509506.1:c.-558_-553del (IL10)	XP_011507808.1:n.-558_-553del
NM_153758.3:c.-35+1913_-35+1918del (IL19)	NP_715639.1:n.-35+1913_-35+1918del
NM_001393490.1:c.-149+2161_-149+2166del (IL19)	NP_001380419.1:n.-149+2161_-149+2166del
NM_153758.5:c.-149+1913_-149+1918del (IL19) MANE Select	NP_715639.2:n.-149+1913_-149+1918del