Canonical Allele Identifier: CA528574922

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1454979310
• gnomAD v2: 1-206946354-A-AT
• gnomAD v3: 1-206773009-A-AT
• gnomAD v4: 1-206773009-A-AT
• MyVariant Identifiers: chr1:g.206946354_206946355insT (hg19) ; chr1:g.206773009_206773010insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773009_206773010insT , CM000663.2:g.206773009_206773010insT	GRCh38
NC_000001.10:g.206946354_206946355insT , CM000663.1:g.206946354_206946355insT	GRCh37
NC_000001.9:g.205012977_205012978insT	NCBI36
NG_012088.1:g.4485_4486insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.-15+670_-15+671insA (IL10)	ENSP00000499588.1:n.-15+670_-15+671insA
ENST00000659642.2:c.-692_-691insA (IL10)	ENSP00000499509.1:n.-692_-691insA
ENST00000664374.2:c.-14-678_-14-677insA (IL10)	ENSP00000499664.1:n.-14-678_-14-677insA
ENST00000659997.3:c.-149+1931_-149+1932insT (IL19) MANE Select	ENSP00000499459.2:n.-149+1931_-149+1932in...
ENST00000656872.2:c.-149+2179_-149+2180insT (IL19)	ENSP00000499487.2:n.-149+2179_-149+2180in...
ENST00000659065.1:c.-15+670_-15+671insA (IL10)	ENSP00000499588.1:n.-15+670_-15+671insA
ENST00000659642.1:c.-692_-691insA (IL10)	ENSP00000499509.1:n.-692_-691insA
ENST00000659997.2:c.-149+1931_-149+1932insT (IL19)	ENSP00000499459.2:n.-149+1931_-149+1932in...
ENST00000662320.1:n.67+2179_67+2180insT (IL19)
ENST00000664374.1:c.-14-678_-14-677insA (IL10)	ENSP00000499664.1:n.-14-678_-14-677insA
XM_011509506.1:c.-575_-574insA (IL10)	XP_011507808.1:n.-575_-574insA
NM_153758.3:c.-35+1931_-35+1932insT (IL19)	NP_715639.1:n.-35+1931_-35+1932insT
NM_001393490.1:c.-149+2179_-149+2180insT (IL19)	NP_001380419.1:n.-149+2179_-149+2180insT
NM_153758.5:c.-149+1931_-149+1932insT (IL19) MANE Select	NP_715639.2:n.-149+1931_-149+1932insT