Canonical Allele Identifier: CA2602794073
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072229_111072242del , CM000667.2:g.111072229_111072242del GRCh38
NC_000005.9:g.110407927_110407940del , CM000667.1:g.110407927_110407940del GRCh37
NC_000005.8:g.110435826_110435839del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.171+168_171+181del MANE Select ENSP00000339804.3:n.171+168_171+181del
ENST00000344895.3:c.171+168_171+181del ENSP00000339804.3:n.171+168_171+181del
ENST00000420978.6:c.171+168_171+181del ENSP00000399099.2:n.171+168_171+181del
NM_033035.4:c.171+168_171+181del NP_149024.1:n.171+168_171+181del
NR_045089.1:n.1575+168_1575+181del
NM_033035.5:c.171+168_171+181del MANE Select NP_149024.1:n.171+168_171+181del
NR_045089.2:n.1593+168_1593+181del