Canonical Allele Identifier: CA2483125882

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206769039A= , CM000663.2:g.206769039A=	GRCh38
NC_000001.10:g.206942384A= , CM000663.1:g.206942384A=	GRCh37
NC_000001.9:g.205009007A=	NCBI36
NG_012088.1:g.8456T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.1139T=
ENST00000471071.2:c.190-311T=	ENSP00000493073.2:n.190-311T=
ENST00000640756.2:n.255-311T=
ENST00000659065.2:c.328-311T=	ENSP00000499588.1:n.328-311T=
ENST00000659642.2:c.328-311T=	ENSP00000499509.1:n.328-311T=
ENST00000664374.2:c.328-311T=	ENSP00000499664.1:n.328-311T=
ENST00000640756.1:n.244-311T=
ENST00000659065.1:c.328-311T=	ENSP00000499588.1:n.328-311T=
ENST00000659642.1:c.328-311T=	ENSP00000499509.1:n.328-311T=
ENST00000664374.1:c.328-311T=	ENSP00000499664.1:n.328-311T=
ENST00000423557.1:c.445-311T= MANE Select	ENSP00000412237.1:n.445-311T=
ENST00000471071.1:n.360-311T=
NM_000572.2:c.445-311T=	NP_000563.1:n.445-311T=
XM_011509506.1:c.445-311T=	XP_011507808.1:n.445-311T=
NM_000572.3:c.445-311T= MANE Select	NP_000563.1:n.445-311T=
NM_001382624.1:c.190-311T=	NP_001369553.1:n.190-311T=
NR_168466.1:n.742-311T=
NR_168467.1:n.272-311T=