Canonical Allele Identifier: CA2483126648

Linked Data

dbSNP Id: rs1674818549

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771091_206771095dup , CM000663.2:g.206771091_206771095dup GRCh38
NC_000001.10:g.206944436_206944440dup , CM000663.1:g.206944436_206944440dup GRCh37
NC_000001.9:g.205011059_205011063dup NCBI36
NG_012088.1:g.6400_6404dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.95_99dup (IL10)
ENST00000471071.2:c.-66_-62dup (IL10) ENSP00000493073.2:n.-66_-62dup
ENST00000659065.2:c.109-36_109-32dup (IL10) ENSP00000499588.1:n.109-36_109-32dup
ENST00000659642.2:c.109-36_109-32dup (IL10) ENSP00000499509.1:n.109-36_109-32dup
ENST00000664374.2:c.109-36_109-32dup (IL10) ENSP00000499664.1:n.109-36_109-32dup
ENST00000659997.3:c.-149+13_-149+17dup (IL19) MANE Select ENSP00000499459.2:n.-149+13_-149+17dup
ENST00000656872.2:c.-149+261_-149+265dup (IL19) ENSP00000499487.2:n.-149+261_-149+265dup
ENST00000659065.1:c.109-36_109-32dup (IL10) ENSP00000499588.1:n.109-36_109-32dup
ENST00000659642.1:c.109-36_109-32dup (IL10) ENSP00000499509.1:n.109-36_109-32dup
ENST00000659997.2:c.-149+13_-149+17dup (IL19) ENSP00000499459.2:n.-149+13_-149+17dup
ENST00000662320.1:n.67+261_67+265dup (IL19)
ENST00000664374.1:c.109-36_109-32dup (IL10) ENSP00000499664.1:n.109-36_109-32dup
ENST00000367099.3:n.95_99dup (IL10)
ENST00000423557.1:c.226-36_226-32dup (IL10) MANE Select ENSP00000412237.1:n.226-36_226-32dup
ENST00000471071.1:n.105_109dup (IL10)
NM_000572.2:c.226-36_226-32dup (IL10) NP_000563.1:n.226-36_226-32dup
XM_011509506.1:c.226-36_226-32dup (IL10) XP_011507808.1:n.226-36_226-32dup
NM_000572.3:c.226-36_226-32dup (IL10) MANE Select NP_000563.1:n.226-36_226-32dup
NM_153758.3:c.-35+13_-35+17dup (IL19) NP_715639.1:n.-35+13_-35+17dup
NM_001382624.1:c.-66_-62dup (IL10) NP_001369553.1:n.-66_-62dup
NM_001393490.1:c.-149+261_-149+265dup (IL19) NP_001380419.1:n.-149+261_-149+265dup
NM_153758.5:c.-149+13_-149+17dup (IL19) MANE Select NP_715639.2:n.-149+13_-149+17dup
NR_168466.1:n.285-36_285-32dup (IL10)