Canonical Allele Identifier: CA2483125759

Gene: IL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768658A= , CM000663.2:g.206768658A=	GRCh38
NC_000001.10:g.206942003A= , CM000663.1:g.206942003A=	GRCh37
NC_000001.9:g.205008626A=	NCBI36
NG_012088.1:g.8837T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1520T=
ENST00000471071.2:c.260T=	ENSP00000493073.2:p.Met87=
ENST00000640756.2:n.325T=
ENST00000659065.2:c.398T=	ENSP00000499588.1:p.Met133=
ENST00000659642.2:c.398T=	ENSP00000499509.1:p.Met133=
ENST00000664374.2:c.398T=	ENSP00000499664.1:p.Met133=
ENST00000640756.1:n.314T=
ENST00000659065.1:c.398T=	ENSP00000499588.1:p.Met133=
ENST00000659642.1:c.398T=	ENSP00000499509.1:p.Met133=
ENST00000664374.1:c.398T=	ENSP00000499664.1:p.Met133=
ENST00000423557.1:c.515T= MANE Select	ENSP00000412237.1:p.Met172=
NM_000572.2:c.515T=	NP_000563.1:p.Met172=
XM_011509506.1:c.515T=	XP_011507808.1:p.Met172=
NM_000572.3:c.515T= MANE Select	NP_000563.1:p.Met172=
NM_001382624.1:c.260T=	NP_001369553.1:p.Met87=
NR_168466.1:n.812T=
NR_168467.1:n.342T=