Canonical Allele Identifier: CA422931377

Gene: IL10 IL19

Linked Data

• MyVariant Identifiers: chr1:g.206944273G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770928G>A , CM000663.2:g.206770928G>A	GRCh38
NC_000001.10:g.206944273G>A , CM000663.1:g.206944273G>A	GRCh37
NC_000001.9:g.205010896G>A	NCBI36
NG_012088.1:g.6567C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.262C>T (IL10)
ENST00000471071.2:c.102C>T (IL10)	ENSP00000493073.2:p.Leu34=
ENST00000659065.2:c.240C>T (IL10)	ENSP00000499588.1:p.Leu80=
ENST00000659642.2:c.240C>T (IL10)	ENSP00000499509.1:p.Leu80=
ENST00000664374.2:c.240C>T (IL10)	ENSP00000499664.1:p.Leu80=
ENST00000659997.3:c.-299G>A (IL19) MANE Select	ENSP00000499459.2:n.-299G>A
ENST00000656872.2:c.-149+98G>A (IL19)	ENSP00000499487.2:n.-149+98G>A
ENST00000659065.1:c.240C>T (IL10)	ENSP00000499588.1:p.Leu80=
ENST00000659642.1:c.240C>T (IL10)	ENSP00000499509.1:p.Leu80=
ENST00000659997.2:c.-299G>A (IL19)	ENSP00000499459.2:n.-299G>A
ENST00000662320.1:n.67+98G>A (IL19)
ENST00000664374.1:c.240C>T (IL10)	ENSP00000499664.1:p.Leu80=
ENST00000367099.3:n.262C>T (IL10)
ENST00000423557.1:c.357C>T (IL10) MANE Select	ENSP00000412237.1:p.Leu119=
ENST00000471071.1:n.272C>T (IL10)
NM_000572.2:c.357C>T (IL10)	NP_000563.1:p.Leu119=
XM_011509506.1:c.357C>T (IL10)	XP_011507808.1:p.Leu119=
NM_000572.3:c.357C>T (IL10) MANE Select	NP_000563.1:p.Leu119=
NM_153758.3:c.-185G>A (IL19)	NP_715639.1:n.-185G>A
NM_001382624.1:c.102C>T (IL10)	NP_001369553.1:p.Leu34=
NM_001393490.1:c.-149+98G>A (IL19)	NP_001380419.1:n.-149+98G>A
NM_153758.5:c.-299G>A (IL19) MANE Select	NP_715639.2:n.-299G>A
NR_168466.1:n.416C>T (IL10)