Canonical Allele Identifier: CA344481586

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942009G>T (hg19) ; chr1:g.206768664G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768664G>T , CM000663.2:g.206768664G>T	GRCh38
NC_000001.10:g.206942009G>T , CM000663.1:g.206942009G>T	GRCh37
NC_000001.9:g.205008632G>T	NCBI36
NG_012088.1:g.8831C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1514C>A
ENST00000471071.2:c.254C>A	ENSP00000493073.2:p.Ala85Asp
ENST00000640756.2:n.319C>A
ENST00000659065.2:c.392C>A	ENSP00000499588.1:p.Ala131Asp
ENST00000659642.2:c.392C>A	ENSP00000499509.1:p.Ala131Asp
ENST00000664374.2:c.392C>A	ENSP00000499664.1:p.Ala131Asp
ENST00000640756.1:n.308C>A
ENST00000659065.1:c.392C>A	ENSP00000499588.1:p.Ala131Asp
ENST00000659642.1:c.392C>A	ENSP00000499509.1:p.Ala131Asp
ENST00000664374.1:c.392C>A	ENSP00000499664.1:p.Ala131Asp
ENST00000423557.1:c.509C>A MANE Select	ENSP00000412237.1:p.Ala170Asp
NM_000572.2:c.509C>A	NP_000563.1:p.Ala170Asp
XM_011509506.1:c.509C>A	XP_011507808.1:p.Ala170Asp
NM_000572.3:c.509C>A MANE Select	NP_000563.1:p.Ala170Asp
NM_001382624.1:c.254C>A	NP_001369553.1:p.Ala85Asp
NR_168466.1:n.806C>A
NR_168467.1:n.336C>A