Canonical Allele Identifier: CA10699284

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770767T>A , CM000663.2:g.206770767T>A	GRCh38
NC_000001.10:g.206944112T>A , CM000663.1:g.206944112T>A	GRCh37
NC_000001.9:g.205010735T>A	NCBI36
NG_012088.1:g.6728A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000572.3:c.378+140A>T (IL10) MANE Select	NP_000563.1:n.378+140A>T
ENST00000423557.1:c.378+140A>T (IL10) MANE Select	ENSP00000412237.1:n.378+140A>T
NM_000572.2:c.378+140A>T (IL10)	NP_000563.1:n.378+140A>T
NM_001382624.1:c.123+140A>T (IL10)	NP_001369553.1:n.123+140A>T
NR_168466.1:n.437+140A>T (IL10)
ENST00000367099.3:n.283+140A>T (IL10)
ENST00000367099.4:n.283+140A>T (IL10)
ENST00000471071.1:n.293+140A>T (IL10)
ENST00000471071.2:c.123+140A>T (IL10)	ENSP00000493073.2:n.123+140A>T
ENST00000656872.2:c.-212T>A (IL19)	ENSP00000499487.2:n.-212T>A
ENST00000659065.1:c.261+140A>T (IL10)	ENSP00000499588.1:n.261+140A>T
ENST00000659065.2:c.261+140A>T (IL10)	ENSP00000499588.1:n.261+140A>T
ENST00000659642.1:c.261+140A>T (IL10)	ENSP00000499509.1:n.261+140A>T
ENST00000659642.2:c.261+140A>T (IL10)	ENSP00000499509.1:n.261+140A>T
ENST00000659997.2:c.-460T>A (IL19)	ENSP00000499459.2:n.-460T>A
ENST00000662320.1:n.4T>A (IL19)
ENST00000664374.1:c.261+140A>T (IL10)	ENSP00000499664.1:n.261+140A>T
ENST00000664374.2:c.261+140A>T (IL10)	ENSP00000499664.1:n.261+140A>T
XM_011509506.1:c.378+140A>T (IL10)	XP_011507808.1:n.378+140A>T