Canonical Allele Identifier: CA730538070

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1175010475
• gnomAD v3: 1-206771154-CG-C
• gnomAD v4: 1-206771154-CG-C
• MyVariant Identifiers: chr1:g.206944500del (hg19) ; chr1:g.206771155del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771155del , CM000663.2:g.206771155del	GRCh38
NC_000001.10:g.206944500del , CM000663.1:g.206944500del	GRCh37
NC_000001.9:g.205011123del	NCBI36
NG_012088.1:g.6340del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.35del (IL10)
ENST00000471071.2:c.-126del (IL10)	ENSP00000493073.2:n.-126del
ENST00000659065.2:c.109-96del (IL10)	ENSP00000499588.1:n.109-96del
ENST00000659642.2:c.109-96del (IL10)	ENSP00000499509.1:n.109-96del
ENST00000664374.2:c.109-96del (IL10)	ENSP00000499664.1:n.109-96del
ENST00000659997.3:c.-149+77del (IL19) MANE Select	ENSP00000499459.2:n.-149+77del
ENST00000656872.2:c.-149+325del (IL19)	ENSP00000499487.2:n.-149+325del
ENST00000659065.1:c.109-96del (IL10)	ENSP00000499588.1:n.109-96del
ENST00000659642.1:c.109-96del (IL10)	ENSP00000499509.1:n.109-96del
ENST00000659997.2:c.-149+77del (IL19)	ENSP00000499459.2:n.-149+77del
ENST00000662320.1:n.67+325del (IL19)
ENST00000664374.1:c.109-96del (IL10)	ENSP00000499664.1:n.109-96del
ENST00000367099.3:n.35del (IL10)
ENST00000423557.1:c.226-96del (IL10) MANE Select	ENSP00000412237.1:n.226-96del
ENST00000471071.1:n.45del (IL10)
NM_000572.2:c.226-96del (IL10)	NP_000563.1:n.226-96del
XM_011509506.1:c.226-96del (IL10)	XP_011507808.1:n.226-96del
NM_000572.3:c.226-96del (IL10) MANE Select	NP_000563.1:n.226-96del
NM_153758.3:c.-35+77del (IL19)	NP_715639.1:n.-35+77del
NM_001382624.1:c.-126del (IL10)	NP_001369553.1:n.-126del
NM_001393490.1:c.-149+325del (IL19)	NP_001380419.1:n.-149+325del
NM_153758.5:c.-149+77del (IL19) MANE Select	NP_715639.2:n.-149+77del
NR_168466.1:n.285-96del (IL10)