Canonical Allele Identifier: CA528574857

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1397820081
• gnomAD v2: 1-206944867-GGCTCTGGCCC-G
• gnomAD v4: 1-206771522-GGCTCTGGCCC-G
• MyVariant Identifiers: chr1:g.206944868_206944877del (hg19) ; chr1:g.206771523_206771532del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771523_206771532del , CM000663.2:g.206771523_206771532del	GRCh38
NC_000001.10:g.206944868_206944877del , CM000663.1:g.206944868_206944877del	GRCh37
NC_000001.9:g.205011491_205011500del	NCBI36
NG_012088.1:g.5963_5972del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.49-117_49-108del (IL10)	ENSP00000499588.1:n.49-117_49-108del
ENST00000659642.2:c.49-117_49-108del (IL10)	ENSP00000499509.1:n.49-117_49-108del
ENST00000664374.2:c.49-117_49-108del (IL10)	ENSP00000499664.1:n.49-117_49-108del
ENST00000659997.3:c.-149+445_-149+454del (IL19) MANE Select	ENSP00000499459.2:n.-149+445_-149+454del
ENST00000656872.2:c.-149+693_-149+702del (IL19)	ENSP00000499487.2:n.-149+693_-149+702del
ENST00000659065.1:c.49-117_49-108del (IL10)	ENSP00000499588.1:n.49-117_49-108del
ENST00000659642.1:c.49-117_49-108del (IL10)	ENSP00000499509.1:n.49-117_49-108del
ENST00000659997.2:c.-149+445_-149+454del (IL19)	ENSP00000499459.2:n.-149+445_-149+454del
ENST00000662320.1:n.67+693_67+702del (IL19)
ENST00000664374.1:c.49-117_49-108del (IL10)	ENSP00000499664.1:n.49-117_49-108del
ENST00000423557.1:c.166-117_166-108del (IL10) MANE Select	ENSP00000412237.1:n.166-117_166-108del
NM_000572.2:c.166-117_166-108del (IL10)	NP_000563.1:n.166-117_166-108del
XM_011509506.1:c.166-117_166-108del (IL10)	XP_011507808.1:n.166-117_166-108del
NM_000572.3:c.166-117_166-108del (IL10) MANE Select	NP_000563.1:n.166-117_166-108del
NM_153758.3:c.-35+445_-35+454del (IL19)	NP_715639.1:n.-35+445_-35+454del
NM_001393490.1:c.-149+693_-149+702del (IL19)	NP_001380419.1:n.-149+693_-149+702del
NM_153758.5:c.-149+445_-149+454del (IL19) MANE Select	NP_715639.2:n.-149+445_-149+454del
NR_168466.1:n.225-117_225-108del (IL10)