Canonical Allele Identifier: CA1145230536

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206769110C= , CM000663.2:g.206769110C=	GRCh38
NC_000001.10:g.206942455C= , CM000663.1:g.206942455C=	GRCh37
NC_000001.9:g.205009078C=	NCBI36
NG_012088.1:g.8385G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1068G=
ENST00000471071.2:c.190-382G=	ENSP00000493073.2:n.190-382G=
ENST00000640756.2:n.255-382G=
ENST00000659065.2:c.328-382G=	ENSP00000499588.1:n.328-382G=
ENST00000659642.2:c.328-382G=	ENSP00000499509.1:n.328-382G=
ENST00000664374.2:c.328-382G=	ENSP00000499664.1:n.328-382G=
ENST00000640756.1:n.244-382G=
ENST00000659065.1:c.328-382G=	ENSP00000499588.1:n.328-382G=
ENST00000659642.1:c.328-382G=	ENSP00000499509.1:n.328-382G=
ENST00000664374.1:c.328-382G=	ENSP00000499664.1:n.328-382G=
ENST00000423557.1:c.445-382G= MANE Select	ENSP00000412237.1:n.445-382G=
ENST00000471071.1:n.360-382G=
NM_000572.2:c.445-382G=	NP_000563.1:n.445-382G=
XM_011509506.1:c.445-382G=	XP_011507808.1:n.445-382G=
NM_000572.3:c.445-382G= MANE Select	NP_000563.1:n.445-382G=
NM_001382624.1:c.190-382G=	NP_001369553.1:n.190-382G=
NR_168466.1:n.742-382G=
NR_168467.1:n.272-382G=