Canonical Allele Identifier: CA2483125813

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768843C= , CM000663.2:g.206768843C=	GRCh38
NC_000001.10:g.206942188C= , CM000663.1:g.206942188C=	GRCh37
NC_000001.9:g.205008811C=	NCBI36
NG_012088.1:g.8652G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1335G=
ENST00000471071.2:c.190-115G=	ENSP00000493073.2:n.190-115G=
ENST00000640756.2:n.255-115G=
ENST00000659065.2:c.328-115G=	ENSP00000499588.1:n.328-115G=
ENST00000659642.2:c.328-115G=	ENSP00000499509.1:n.328-115G=
ENST00000664374.2:c.328-115G=	ENSP00000499664.1:n.328-115G=
ENST00000640756.1:n.244-115G=
ENST00000659065.1:c.328-115G=	ENSP00000499588.1:n.328-115G=
ENST00000659642.1:c.328-115G=	ENSP00000499509.1:n.328-115G=
ENST00000664374.1:c.328-115G=	ENSP00000499664.1:n.328-115G=
ENST00000423557.1:c.445-115G= MANE Select	ENSP00000412237.1:n.445-115G=
ENST00000471071.1:n.360-115G=
NM_000572.2:c.445-115G=	NP_000563.1:n.445-115G=
XM_011509506.1:c.445-115G=	XP_011507808.1:n.445-115G=
NM_000572.3:c.445-115G= MANE Select	NP_000563.1:n.445-115G=
NM_001382624.1:c.190-115G=	NP_001369553.1:n.190-115G=
NR_168466.1:n.742-115G=
NR_168467.1:n.272-115G=