Canonical Allele Identifier: CA2650218553

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771155_206771156del , CM000663.2:g.206771155_206771156del GRCh38
NC_000001.10:g.206944500_206944501del , CM000663.1:g.206944500_206944501del GRCh37
NC_000001.9:g.205011123_205011124del NCBI36
NG_012088.1:g.6339_6340del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.34_35del (IL10)
ENST00000471071.2:c.-127_-126del (IL10) ENSP00000493073.2:n.-127_-126del
ENST00000659065.2:c.109-97_109-96del (IL10) ENSP00000499588.1:n.109-97_109-96del
ENST00000659642.2:c.109-97_109-96del (IL10) ENSP00000499509.1:n.109-97_109-96del
ENST00000664374.2:c.109-97_109-96del (IL10) ENSP00000499664.1:n.109-97_109-96del
ENST00000659997.3:c.-149+77_-149+78del (IL19) MANE Select ENSP00000499459.2:n.-149+77_-149+78del
ENST00000656872.2:c.-149+325_-149+326del (IL19) ENSP00000499487.2:n.-149+325_-149+326del
ENST00000659065.1:c.109-97_109-96del (IL10) ENSP00000499588.1:n.109-97_109-96del
ENST00000659642.1:c.109-97_109-96del (IL10) ENSP00000499509.1:n.109-97_109-96del
ENST00000659997.2:c.-149+77_-149+78del (IL19) ENSP00000499459.2:n.-149+77_-149+78del
ENST00000662320.1:n.67+325_67+326del (IL19)
ENST00000664374.1:c.109-97_109-96del (IL10) ENSP00000499664.1:n.109-97_109-96del
ENST00000367099.3:n.34_35del (IL10)
ENST00000423557.1:c.226-97_226-96del (IL10) MANE Select ENSP00000412237.1:n.226-97_226-96del
ENST00000471071.1:n.44_45del (IL10)
NM_000572.2:c.226-97_226-96del (IL10) NP_000563.1:n.226-97_226-96del
XM_011509506.1:c.226-97_226-96del (IL10) XP_011507808.1:n.226-97_226-96del
NM_000572.3:c.226-97_226-96del (IL10) MANE Select NP_000563.1:n.226-97_226-96del
NM_153758.3:c.-35+77_-35+78del (IL19) NP_715639.1:n.-35+77_-35+78del
NM_001382624.1:c.-127_-126del (IL10) NP_001369553.1:n.-127_-126del
NM_001393490.1:c.-149+325_-149+326del (IL19) NP_001380419.1:n.-149+325_-149+326del
NM_153758.5:c.-149+77_-149+78del (IL19) MANE Select NP_715639.2:n.-149+77_-149+78del
NR_168466.1:n.285-97_285-96del (IL10)