Canonical Allele Identifier: CA2650218788

Linked Data

dbSNP Id: rs1009464908

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771539del , CM000663.2:g.206771539del GRCh38
NC_000001.10:g.206944884del , CM000663.1:g.206944884del GRCh37
NC_000001.9:g.205011507del NCBI36
NG_012088.1:g.5962del

Transcript Alleles

HGVS Amino-acid change
ENST00000659065.2:c.49-118del (IL10) ENSP00000499588.1:n.49-118del
ENST00000659642.2:c.49-118del (IL10) ENSP00000499509.1:n.49-118del
ENST00000664374.2:c.49-118del (IL10) ENSP00000499664.1:n.49-118del
ENST00000659997.3:c.-149+461del (IL19) MANE Select ENSP00000499459.2:n.-149+461del
ENST00000656872.2:c.-149+709del (IL19) ENSP00000499487.2:n.-149+709del
ENST00000659065.1:c.49-118del (IL10) ENSP00000499588.1:n.49-118del
ENST00000659642.1:c.49-118del (IL10) ENSP00000499509.1:n.49-118del
ENST00000659997.2:c.-149+461del (IL19) ENSP00000499459.2:n.-149+461del
ENST00000662320.1:n.67+709del (IL19)
ENST00000664374.1:c.49-118del (IL10) ENSP00000499664.1:n.49-118del
ENST00000423557.1:c.166-118del (IL10) MANE Select ENSP00000412237.1:n.166-118del
NM_000572.2:c.166-118del (IL10) NP_000563.1:n.166-118del
XM_011509506.1:c.166-118del (IL10) XP_011507808.1:n.166-118del
NM_000572.3:c.166-118del (IL10) MANE Select NP_000563.1:n.166-118del
NM_153758.3:c.-35+461del (IL19) NP_715639.1:n.-35+461del
NM_001393490.1:c.-149+709del (IL19) NP_001380419.1:n.-149+709del
NM_153758.5:c.-149+461del (IL19) MANE Select NP_715639.2:n.-149+461del
NR_168466.1:n.225-118del (IL10)