Canonical Allele Identifier: CA2483127530

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206773170_206773191delinsGGGGGAAGTGGGTAAGAGTAGT , CM000663.2:g.206773170_206773191delinsGGGGGAAGTGGGTAAGAGTAGT GRCh38
NC_000001.10:g.206946515_206946536delinsGGGGGAAGTGGGTAAGAGTAGT , CM000663.1:g.206946515_206946536delinsGGGGGAAGTGGGTAAGAGTAGT GRCh37
NC_000001.9:g.205013138_205013159delinsGGGGGAAGTGGGTAAGAGTAGT NCBI36
NG_012088.1:g.4304_4325delinsACTACTCTTACCCACTTCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000659065.2:c.-15+489_-15+510delinsACTACTCTTACCCACTTCCCCC (IL10) ENSP00000499588.1:n.-15+489_-15+510delinsACTACTCTTACCCACTTCCC...
ENST00000659642.2:c.-873_-852delinsACTACTCTTACCCACTTCCCCC (IL10) ENSP00000499509.1:n.-873_-852delinsACTACTCTTACCCACTTCCCCC
ENST00000664374.2:c.-14-859_-14-838delinsACTACTCTTACCCACTTCCCCC (IL10) ENSP00000499664.1:n.-14-859_-14-838delinsACTACTCTTACCCACTTCCC...
ENST00000659997.3:c.-149+2092_-149+2113delinsGGGGGAAGTGGGTAAGAGTAGT (IL19) MANE Select ENSP00000499459.2:n.-149+2092_-149+2113delinsGGGGGAAGTGGGTAAG...
ENST00000656872.2:c.-149+2340_-149+2361delinsGGGGGAAGTGGGTAAGAGTAGT (IL19) ENSP00000499487.2:n.-149+2340_-149+2361delinsGGGGGAAGTGGGTAAG...
ENST00000659065.1:c.-15+489_-15+510delinsACTACTCTTACCCACTTCCCCC (IL10) ENSP00000499588.1:n.-15+489_-15+510delinsACTACTCTTACCCACTTCCC...
ENST00000659642.1:c.-873_-852delinsACTACTCTTACCCACTTCCCCC (IL10) ENSP00000499509.1:n.-873_-852delinsACTACTCTTACCCACTTCCCCC
ENST00000659997.2:c.-149+2092_-149+2113delinsGGGGGAAGTGGGTAAGAGTAGT (IL19) ENSP00000499459.2:n.-149+2092_-149+2113delinsGGGGGAAGTGGGTAAG...
ENST00000662320.1:n.67+2340_67+2361delinsGGGGGAAGTGGGTAAGAGTAGT (IL19)
ENST00000664374.1:c.-14-859_-14-838delinsACTACTCTTACCCACTTCCCCC (IL10) ENSP00000499664.1:n.-14-859_-14-838delinsACTACTCTTACCCACTTCCC...
XM_011509506.1:c.-756_-735delinsACTACTCTTACCCACTTCCCCC (IL10) XP_011507808.1:n.-756_-735delinsACTACTCTTACCCACTTCCCCC
NM_153758.3:c.-35+2092_-35+2113delinsGGGGGAAGTGGGTAAGAGTAGT (IL19) NP_715639.1:n.-35+2092_-35+2113delinsGGGGGAAGTGGGTAAGAGTAGT
NM_001393490.1:c.-149+2340_-149+2361delinsGGGGGAAGTGGGTAAGAGTAGT (IL19) NP_001380419.1:n.-149+2340_-149+2361delinsGGGGGAAGTGGGTAAGAGT...
NM_153758.5:c.-149+2092_-149+2113delinsGGGGGAAGTGGGTAAGAGTAGT (IL19) MANE Select NP_715639.2:n.-149+2092_-149+2113delinsGGGGGAAGTGGGTAAGAGTAGT...