Canonical Allele Identifier: CA344482066

Gene: IL10 IL19

Linked Data

• MyVariant Identifiers: chr1:g.206944323G>C (hg19) ; chr1:g.206770978G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770978G>C , CM000663.2:g.206770978G>C	GRCh38
NC_000001.10:g.206944323G>C , CM000663.1:g.206944323G>C	GRCh37
NC_000001.9:g.205010946G>C	NCBI36
NG_012088.1:g.6517C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.212C>G (IL10)
ENST00000471071.2:c.52C>G (IL10)	ENSP00000493073.2:p.Pro18Ala
ENST00000659065.2:c.190C>G (IL10)	ENSP00000499588.1:p.Pro64Ala
ENST00000659642.2:c.190C>G (IL10)	ENSP00000499509.1:p.Pro64Ala
ENST00000664374.2:c.190C>G (IL10)	ENSP00000499664.1:p.Pro64Ala
ENST00000659997.3:c.-249G>C (IL19) MANE Select	ENSP00000499459.2:n.-249G>C
ENST00000656872.2:c.-149+148G>C (IL19)	ENSP00000499487.2:n.-149+148G>C
ENST00000659065.1:c.190C>G (IL10)	ENSP00000499588.1:p.Pro64Ala
ENST00000659642.1:c.190C>G (IL10)	ENSP00000499509.1:p.Pro64Ala
ENST00000659997.2:c.-249G>C (IL19)	ENSP00000499459.2:n.-249G>C
ENST00000662320.1:n.67+148G>C (IL19)
ENST00000664374.1:c.190C>G (IL10)	ENSP00000499664.1:p.Pro64Ala
ENST00000367099.3:n.212C>G (IL10)
ENST00000423557.1:c.307C>G (IL10) MANE Select	ENSP00000412237.1:p.Pro103Ala
ENST00000471071.1:n.222C>G (IL10)
NM_000572.2:c.307C>G (IL10)	NP_000563.1:p.Pro103Ala
XM_011509506.1:c.307C>G (IL10)	XP_011507808.1:p.Pro103Ala
NM_000572.3:c.307C>G (IL10) MANE Select	NP_000563.1:p.Pro103Ala
NM_153758.3:c.-135G>C (IL19)	NP_715639.1:n.-135G>C
NM_001382624.1:c.52C>G (IL10)	NP_001369553.1:p.Pro18Ala
NM_001393490.1:c.-149+148G>C (IL19)	NP_001380419.1:n.-149+148G>C
NM_153758.5:c.-249G>C (IL19) MANE Select	NP_715639.2:n.-249G>C
NR_168466.1:n.366C>G (IL10)