Canonical Allele Identifier: CA730538618

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1162004368
• MyVariant Identifiers: chr1:g.206945298del (hg19) ; chr1:g.206771953del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771954del , CM000663.2:g.206771954del	GRCh38
NC_000001.10:g.206945299del , CM000663.1:g.206945299del	GRCh37
NC_000001.9:g.205011922del	NCBI36
NG_012088.1:g.5542del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.48+318del (IL10)	ENSP00000499588.1:n.48+318del
ENST00000659642.2:c.48+318del (IL10)	ENSP00000499509.1:n.48+318del
ENST00000664374.2:c.48+318del (IL10)	ENSP00000499664.1:n.48+318del
ENST00000659997.3:c.-149+876del (IL19) MANE Select	ENSP00000499459.2:n.-149+876del
ENST00000656872.2:c.-149+1124del (IL19)	ENSP00000499487.2:n.-149+1124del
ENST00000659065.1:c.48+318del (IL10)	ENSP00000499588.1:n.48+318del
ENST00000659642.1:c.48+318del (IL10)	ENSP00000499509.1:n.48+318del
ENST00000659997.2:c.-149+876del (IL19)	ENSP00000499459.2:n.-149+876del
ENST00000662320.1:n.67+1124del (IL19)
ENST00000664374.1:c.48+318del (IL10)	ENSP00000499664.1:n.48+318del
ENST00000423557.1:c.165+318del (IL10) MANE Select	ENSP00000412237.1:n.165+318del
NM_000572.2:c.165+318del (IL10)	NP_000563.1:n.165+318del
XM_011509506.1:c.165+318del (IL10)	XP_011507808.1:n.165+318del
NM_000572.3:c.165+318del (IL10) MANE Select	NP_000563.1:n.165+318del
NM_153758.3:c.-35+876del (IL19)	NP_715639.1:n.-35+876del
NM_001393490.1:c.-149+1124del (IL19)	NP_001380419.1:n.-149+1124del
NM_153758.5:c.-149+876del (IL19) MANE Select	NP_715639.2:n.-149+876del
NR_168466.1:n.224+318del (IL10)