Canonical Allele Identifier: CA422931372

Gene: IL10 IL19

Linked Data

• MyVariant Identifiers: chr1:g.206944267C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770922C>A , CM000663.2:g.206770922C>A	GRCh38
NC_000001.10:g.206944267C>A , CM000663.1:g.206944267C>A	GRCh37
NC_000001.9:g.205010890C>A	NCBI36
NG_012088.1:g.6573G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.268G>T (IL10)
ENST00000471071.2:c.108G>T (IL10)	ENSP00000493073.2:p.Leu36=
ENST00000659065.2:c.246G>T (IL10)	ENSP00000499588.1:p.Leu82=
ENST00000659642.2:c.246G>T (IL10)	ENSP00000499509.1:p.Leu82=
ENST00000664374.2:c.246G>T (IL10)	ENSP00000499664.1:p.Leu82=
ENST00000659997.3:c.-305C>A (IL19) MANE Select	ENSP00000499459.2:n.-305C>A
ENST00000656872.2:c.-149+92C>A (IL19)	ENSP00000499487.2:n.-149+92C>A
ENST00000659065.1:c.246G>T (IL10)	ENSP00000499588.1:p.Leu82=
ENST00000659642.1:c.246G>T (IL10)	ENSP00000499509.1:p.Leu82=
ENST00000659997.2:c.-305C>A (IL19)	ENSP00000499459.2:n.-305C>A
ENST00000662320.1:n.67+92C>A (IL19)
ENST00000664374.1:c.246G>T (IL10)	ENSP00000499664.1:p.Leu82=
ENST00000367099.3:n.268G>T (IL10)
ENST00000423557.1:c.363G>T (IL10) MANE Select	ENSP00000412237.1:p.Leu121=
ENST00000471071.1:n.278G>T (IL10)
NM_000572.2:c.363G>T (IL10)	NP_000563.1:p.Leu121=
XM_011509506.1:c.363G>T (IL10)	XP_011507808.1:p.Leu121=
NM_000572.3:c.363G>T (IL10) MANE Select	NP_000563.1:p.Leu121=
NM_153758.3:c.-191C>A (IL19)	NP_715639.1:n.-191C>A
NM_001382624.1:c.108G>T (IL10)	NP_001369553.1:p.Leu36=
NM_001393490.1:c.-149+92C>A (IL19)	NP_001380419.1:n.-149+92C>A
NM_153758.5:c.-305C>A (IL19) MANE Select	NP_715639.2:n.-305C>A
NR_168466.1:n.422G>T (IL10)