Canonical Allele Identifier: CA1572617327
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072436_111072439delinsCCAG , CM000667.2:g.111072436_111072439delinsCCAG GRCh38
NC_000005.9:g.110408134_110408137delinsCCAG , CM000667.1:g.110408134_110408137delinsCCAG GRCh37
NC_000005.8:g.110436033_110436036delinsCCAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+375_171+378delinsCCAG MANE Select ENSP00000339804.3:n.171+375_171+378delinsCCAG
ENST00000344895.3:c.171+375_171+378delinsCCAG ENSP00000339804.3:n.171+375_171+378delinsCCAG
ENST00000420978.6:c.171+375_171+378delinsCCAG ENSP00000399099.2:n.171+375_171+378delinsCCAG
NM_033035.4:c.171+375_171+378delinsCCAG NP_149024.1:n.171+375_171+378delinsCCAG
NR_045089.1:n.1575+375_1575+378delinsCCAG
NM_033035.5:c.171+375_171+378delinsCCAG MANE Select NP_149024.1:n.171+375_171+378delinsCCAG
NR_045089.2:n.1593+375_1593+378delinsCCAG