Canonical Allele Identifier: CA2483126614

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770984G= , CM000663.2:g.206770984G=	GRCh38
NC_000001.10:g.206944329G= , CM000663.1:g.206944329G=	GRCh37
NC_000001.9:g.205010952G=	NCBI36
NG_012088.1:g.6511C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.206C= (IL10)
ENST00000471071.2:c.46C= (IL10)	ENSP00000493073.2:p.Gln16=
ENST00000659065.2:c.184C= (IL10)	ENSP00000499588.1:p.Gln62=
ENST00000659642.2:c.184C= (IL10)	ENSP00000499509.1:p.Gln62=
ENST00000664374.2:c.184C= (IL10)	ENSP00000499664.1:p.Gln62=
ENST00000659997.3:c.-243G= (IL19) MANE Select	ENSP00000499459.2:n.-243G=
ENST00000656872.2:c.-149+154G= (IL19)	ENSP00000499487.2:n.-149+154G=
ENST00000659065.1:c.184C= (IL10)	ENSP00000499588.1:p.Gln62=
ENST00000659642.1:c.184C= (IL10)	ENSP00000499509.1:p.Gln62=
ENST00000659997.2:c.-243G= (IL19)	ENSP00000499459.2:n.-243G=
ENST00000662320.1:n.67+154G= (IL19)
ENST00000664374.1:c.184C= (IL10)	ENSP00000499664.1:p.Gln62=
ENST00000367099.3:n.206C= (IL10)
ENST00000423557.1:c.301C= (IL10) MANE Select	ENSP00000412237.1:p.Gln101=
ENST00000471071.1:n.216C= (IL10)
NM_000572.2:c.301C= (IL10)	NP_000563.1:p.Gln101=
XM_011509506.1:c.301C= (IL10)	XP_011507808.1:p.Gln101=
NM_000572.3:c.301C= (IL10) MANE Select	NP_000563.1:p.Gln101=
NM_153758.3:c.-129G= (IL19)	NP_715639.1:n.-129G=
NM_001382624.1:c.46C= (IL10)	NP_001369553.1:p.Gln16=
NM_001393490.1:c.-149+154G= (IL19)	NP_001380419.1:n.-149+154G=
NM_153758.5:c.-243G= (IL19) MANE Select	NP_715639.2:n.-243G=
NR_168466.1:n.360C= (IL10)