Canonical Allele Identifier: CA2674827869
Gene: TSLP HGNC NCBI

Linked Data

gnomAD v4: 5-111071989-CTG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071992_111071993del , CM000667.2:g.111071992_111071993del GRCh38
NC_000005.9:g.110407690_110407691del , CM000667.1:g.110407690_110407691del GRCh37
NC_000005.8:g.110435589_110435590del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.102_103del MANE Select ENSP00000339804.3:p.Cys34Ter
ENST00000344895.3:c.102_103del ENSP00000339804.3:p.Cys34Ter
ENST00000420978.6:c.102_103del ENSP00000399099.2:p.Cys34Ter
NM_033035.4:c.102_103del NP_149024.1:p.Cys34Ter
NR_045089.1:n.1506_1507del
NM_033035.5:c.102_103del MANE Select NP_149024.1:p.Cys34Ter
NR_045089.2:n.1524_1525del
Search 100 bp 5'
Search 100 bp 3'