Canonical Allele Identifier: CA344481642

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942033T>G (hg19) ; chr1:g.206768688T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768688T>G , CM000663.2:g.206768688T>G	GRCh38
NC_000001.10:g.206942033T>G , CM000663.1:g.206942033T>G	GRCh37
NC_000001.9:g.205008656T>G	NCBI36
NG_012088.1:g.8807A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1490A>C
ENST00000471071.2:c.230A>C	ENSP00000493073.2:p.Asp77Ala
ENST00000640756.2:n.295A>C
ENST00000659065.2:c.368A>C	ENSP00000499588.1:p.Asp123Ala
ENST00000659642.2:c.368A>C	ENSP00000499509.1:p.Asp123Ala
ENST00000664374.2:c.368A>C	ENSP00000499664.1:p.Asp123Ala
ENST00000640756.1:n.284A>C
ENST00000659065.1:c.368A>C	ENSP00000499588.1:p.Asp123Ala
ENST00000659642.1:c.368A>C	ENSP00000499509.1:p.Asp123Ala
ENST00000664374.1:c.368A>C	ENSP00000499664.1:p.Asp123Ala
ENST00000423557.1:c.485A>C MANE Select	ENSP00000412237.1:p.Asp162Ala
NM_000572.2:c.485A>C	NP_000563.1:p.Asp162Ala
XM_011509506.1:c.485A>C	XP_011507808.1:p.Asp162Ala
NM_000572.3:c.485A>C MANE Select	NP_000563.1:p.Asp162Ala
NM_001382624.1:c.230A>C	NP_001369553.1:p.Asp77Ala
NR_168466.1:n.782A>C
NR_168467.1:n.312A>C