Canonical Allele Identifier: CA2483125768

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768701T= , CM000663.2:g.206768701T=	GRCh38
NC_000001.10:g.206942046T= , CM000663.1:g.206942046T=	GRCh37
NC_000001.9:g.205008669T=	NCBI36
NG_012088.1:g.8794A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1477A=
ENST00000471071.2:c.217A=	ENSP00000493073.2:p.Met73=
ENST00000640756.2:n.282A=
ENST00000659065.2:c.355A=	ENSP00000499588.1:p.Met119=
ENST00000659642.2:c.355A=	ENSP00000499509.1:p.Met119=
ENST00000664374.2:c.355A=	ENSP00000499664.1:p.Met119=
ENST00000640756.1:n.271A=
ENST00000659065.1:c.355A=	ENSP00000499588.1:p.Met119=
ENST00000659642.1:c.355A=	ENSP00000499509.1:p.Met119=
ENST00000664374.1:c.355A=	ENSP00000499664.1:p.Met119=
ENST00000423557.1:c.472A= MANE Select	ENSP00000412237.1:p.Met158=
ENST00000471071.1:n.387A=
NM_000572.2:c.472A=	NP_000563.1:p.Met158=
XM_011509506.1:c.472A=	XP_011507808.1:p.Met158=
NM_000572.3:c.472A= MANE Select	NP_000563.1:p.Met158=
NM_001382624.1:c.217A=	NP_001369553.1:p.Met73=
NR_168466.1:n.769A=
NR_168467.1:n.299A=