Canonical Allele Identifier: CA1139982329

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768519A= , CM000663.2:g.206768519A=	GRCh38
NC_000001.10:g.206941864A= , CM000663.1:g.206941864A=	GRCh37
NC_000001.9:g.205008487A=	NCBI36
NG_012088.1:g.8976T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000572.3:c.*117T= MANE Select	NP_000563.1:n.*117T=
ENST00000423557.1:c.*117T= MANE Select	ENSP00000412237.1:n.*117T=
NM_000572.2:c.*117T=	NP_000563.1:n.*117T=
NM_001382624.1:c.*117T=	NP_001369553.1:n.*117T=
NR_168466.1:n.951T=
NR_168467.1:n.481T=
ENST00000367099.4:n.1659T=
ENST00000471071.2:c.*117T=	ENSP00000493073.2:n.*117T=
ENST00000640756.1:n.453T=
ENST00000640756.2:n.464T=
ENST00000659065.1:c.*117T=	ENSP00000499588.1:n.*117T=
ENST00000659065.2:c.*117T=	ENSP00000499588.1:n.*117T=
ENST00000659642.1:c.*117T=	ENSP00000499509.1:n.*117T=
ENST00000659642.2:c.*117T=	ENSP00000499509.1:n.*117T=
ENST00000664374.1:c.*117T=	ENSP00000499664.1:n.*117T=
ENST00000664374.2:c.*117T=	ENSP00000499664.1:n.*117T=
XM_011509506.1:c.*117T=	XP_011507808.1:n.*117T=