Canonical Allele Identifier: CA2483126592

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770910G= , CM000663.2:g.206770910G=	GRCh38
NC_000001.10:g.206944255G= , CM000663.1:g.206944255G=	GRCh37
NC_000001.9:g.205010878G=	NCBI36
NG_012088.1:g.6585C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.280C= (IL10)
ENST00000471071.2:c.120C= (IL10)	ENSP00000493073.2:p.Arg40=
ENST00000659065.2:c.258C= (IL10)	ENSP00000499588.1:p.Arg86=
ENST00000659642.2:c.258C= (IL10)	ENSP00000499509.1:p.Arg86=
ENST00000664374.2:c.258C= (IL10)	ENSP00000499664.1:p.Arg86=
ENST00000659997.3:c.-317G= (IL19) MANE Select	ENSP00000499459.2:n.-317G=
ENST00000656872.2:c.-149+80G= (IL19)	ENSP00000499487.2:n.-149+80G=
ENST00000659065.1:c.258C= (IL10)	ENSP00000499588.1:p.Arg86=
ENST00000659642.1:c.258C= (IL10)	ENSP00000499509.1:p.Arg86=
ENST00000659997.2:c.-317G= (IL19)	ENSP00000499459.2:n.-317G=
ENST00000662320.1:n.67+80G= (IL19)
ENST00000664374.1:c.258C= (IL10)	ENSP00000499664.1:p.Arg86=
ENST00000367099.3:n.280C= (IL10)
ENST00000423557.1:c.375C= (IL10) MANE Select	ENSP00000412237.1:p.Arg125=
ENST00000471071.1:n.290C= (IL10)
NM_000572.2:c.375C= (IL10)	NP_000563.1:p.Arg125=
XM_011509506.1:c.375C= (IL10)	XP_011507808.1:p.Arg125=
NM_000572.3:c.375C= (IL10) MANE Select	NP_000563.1:p.Arg125=
NM_153758.3:c.-203G= (IL19)	NP_715639.1:n.-203G=
NM_001382624.1:c.120C= (IL10)	NP_001369553.1:p.Arg40=
NM_001393490.1:c.-149+80G= (IL19)	NP_001380419.1:n.-149+80G=
NM_153758.5:c.-317G= (IL19) MANE Select	NP_715639.2:n.-317G=
NR_168466.1:n.434C= (IL10)