Canonical Allele Identifier: CA344482185

Gene: IL10 IL19

Linked Data

• MyVariant Identifiers: chr1:g.206944373A>C (hg19) ; chr1:g.206771028A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771028A>C , CM000663.2:g.206771028A>C	GRCh38
NC_000001.10:g.206944373A>C , CM000663.1:g.206944373A>C	GRCh37
NC_000001.9:g.205010996A>C	NCBI36
NG_012088.1:g.6467T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.162T>G (IL10)
ENST00000471071.2:c.2T>G (IL10)	ENSP00000493073.2:p.Met1Arg
ENST00000659065.2:c.140T>G (IL10)	ENSP00000499588.1:p.Met47Arg
ENST00000659642.2:c.140T>G (IL10)	ENSP00000499509.1:p.Met47Arg
ENST00000664374.2:c.140T>G (IL10)	ENSP00000499664.1:p.Met47Arg
ENST00000659997.3:c.-199A>C (IL19) MANE Select	ENSP00000499459.2:n.-199A>C
ENST00000656872.2:c.-149+198A>C (IL19)	ENSP00000499487.2:n.-149+198A>C
ENST00000659065.1:c.140T>G (IL10)	ENSP00000499588.1:p.Met47Arg
ENST00000659642.1:c.140T>G (IL10)	ENSP00000499509.1:p.Met47Arg
ENST00000659997.2:c.-199A>C (IL19)	ENSP00000499459.2:n.-199A>C
ENST00000662320.1:n.67+198A>C (IL19)
ENST00000664374.1:c.140T>G (IL10)	ENSP00000499664.1:p.Met47Arg
ENST00000367099.3:n.162T>G (IL10)
ENST00000423557.1:c.257T>G (IL10) MANE Select	ENSP00000412237.1:p.Met86Arg
ENST00000471071.1:n.172T>G (IL10)
NM_000572.2:c.257T>G (IL10)	NP_000563.1:p.Met86Arg
XM_011509506.1:c.257T>G (IL10)	XP_011507808.1:p.Met86Arg
NM_000572.3:c.257T>G (IL10) MANE Select	NP_000563.1:p.Met86Arg
NM_153758.3:c.-85A>C (IL19)	NP_715639.1:n.-85A>C
NM_001382624.1:c.2T>G (IL10)	NP_001369553.1:p.Met1Arg
NM_001393490.1:c.-149+198A>C (IL19)	NP_001380419.1:n.-149+198A>C
NM_153758.5:c.-199A>C (IL19) MANE Select	NP_715639.2:n.-199A>C
NR_168466.1:n.316T>G (IL10)