Canonical Allele Identifier: CA344482175

Gene: IL10 IL19

Linked Data

• MyVariant Identifiers: chr1:g.206944369G>C (hg19) ; chr1:g.206771024G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771024G>C , CM000663.2:g.206771024G>C	GRCh38
NC_000001.10:g.206944369G>C , CM000663.1:g.206944369G>C	GRCh37
NC_000001.9:g.205010992G>C	NCBI36
NG_012088.1:g.6471C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.166C>G (IL10)
ENST00000471071.2:c.6C>G (IL10)	ENSP00000493073.2:p.Ile2Met
ENST00000659065.2:c.144C>G (IL10)	ENSP00000499588.1:p.Ile48Met
ENST00000659642.2:c.144C>G (IL10)	ENSP00000499509.1:p.Ile48Met
ENST00000664374.2:c.144C>G (IL10)	ENSP00000499664.1:p.Ile48Met
ENST00000659997.3:c.-203G>C (IL19) MANE Select	ENSP00000499459.2:n.-203G>C
ENST00000656872.2:c.-149+194G>C (IL19)	ENSP00000499487.2:n.-149+194G>C
ENST00000659065.1:c.144C>G (IL10)	ENSP00000499588.1:p.Ile48Met
ENST00000659642.1:c.144C>G (IL10)	ENSP00000499509.1:p.Ile48Met
ENST00000659997.2:c.-203G>C (IL19)	ENSP00000499459.2:n.-203G>C
ENST00000662320.1:n.67+194G>C (IL19)
ENST00000664374.1:c.144C>G (IL10)	ENSP00000499664.1:p.Ile48Met
ENST00000367099.3:n.166C>G (IL10)
ENST00000423557.1:c.261C>G (IL10) MANE Select	ENSP00000412237.1:p.Ile87Met
ENST00000471071.1:n.176C>G (IL10)
NM_000572.2:c.261C>G (IL10)	NP_000563.1:p.Ile87Met
XM_011509506.1:c.261C>G (IL10)	XP_011507808.1:p.Ile87Met
NM_000572.3:c.261C>G (IL10) MANE Select	NP_000563.1:p.Ile87Met
NM_153758.3:c.-89G>C (IL19)	NP_715639.1:n.-89G>C
NM_001382624.1:c.6C>G (IL10)	NP_001369553.1:p.Ile2Met
NM_001393490.1:c.-149+194G>C (IL19)	NP_001380419.1:n.-149+194G>C
NM_153758.5:c.-203G>C (IL19) MANE Select	NP_715639.2:n.-203G>C
NR_168466.1:n.320C>G (IL10)