Canonical Allele Identifier: CA2650218507

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206770949dup , CM000663.2:g.206770949dup GRCh38
NC_000001.10:g.206944294dup , CM000663.1:g.206944294dup GRCh37
NC_000001.9:g.205010917dup NCBI36
NG_012088.1:g.6550dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.245dup (IL10)
ENST00000471071.2:c.85dup (IL10) ENSP00000493073.2:p.Glu29GlyfsTer20
ENST00000659065.2:c.223dup (IL10) ENSP00000499588.1:p.Glu75GlyfsTer20
ENST00000659642.2:c.223dup (IL10) ENSP00000499509.1:p.Glu75GlyfsTer20
ENST00000664374.2:c.223dup (IL10) ENSP00000499664.1:p.Glu75GlyfsTer20
ENST00000659997.3:c.-278dup (IL19) MANE Select ENSP00000499459.2:n.-278dup
ENST00000656872.2:c.-149+119dup (IL19) ENSP00000499487.2:n.-149+119dup
ENST00000659065.1:c.223dup (IL10) ENSP00000499588.1:p.Glu75GlyfsTer20
ENST00000659642.1:c.223dup (IL10) ENSP00000499509.1:p.Glu75GlyfsTer20
ENST00000659997.2:c.-278dup (IL19) ENSP00000499459.2:n.-278dup
ENST00000662320.1:n.67+119dup (IL19)
ENST00000664374.1:c.223dup (IL10) ENSP00000499664.1:p.Glu75GlyfsTer20
ENST00000367099.3:n.245dup (IL10)
ENST00000423557.1:c.340dup (IL10) MANE Select ENSP00000412237.1:p.Glu114GlyfsTer20
ENST00000471071.1:n.255dup (IL10)
NM_000572.2:c.340dup (IL10) NP_000563.1:p.Glu114GlyfsTer20
XM_011509506.1:c.340dup (IL10) XP_011507808.1:p.Glu114GlyfsTer20
NM_000572.3:c.340dup (IL10) MANE Select NP_000563.1:p.Glu114GlyfsTer20
NM_153758.3:c.-164dup (IL19) NP_715639.1:n.-164dup
NM_001382624.1:c.85dup (IL10) NP_001369553.1:p.Glu29GlyfsTer20
NM_001393490.1:c.-149+119dup (IL19) NP_001380419.1:n.-149+119dup
NM_153758.5:c.-278dup (IL19) MANE Select NP_715639.2:n.-278dup
NR_168466.1:n.399dup (IL10)