Canonical Allele Identifier: CA801887621
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1321662014
gnomAD v3: 5-111072436-CCAG-C
gnomAD v4: 5-111072436-CCAG-C
MyVariant Identifiers: chr5:g.110408135_110408137del (hg19) chr5:g.111072437_111072439del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072437_111072439del , CM000667.2:g.111072437_111072439del GRCh38
NC_000005.9:g.110408135_110408137del , CM000667.1:g.110408135_110408137del GRCh37
NC_000005.8:g.110436034_110436036del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+376_171+378del MANE Select ENSP00000339804.3:n.171+376_171+378del
ENST00000344895.3:c.171+376_171+378del ENSP00000339804.3:n.171+376_171+378del
ENST00000420978.6:c.171+376_171+378del ENSP00000399099.2:n.171+376_171+378del
NM_033035.4:c.171+376_171+378del NP_149024.1:n.171+376_171+378del
NR_045089.1:n.1575+376_1575+378del
NM_033035.5:c.171+376_171+378del MANE Select NP_149024.1:n.171+376_171+378del
NR_045089.2:n.1593+376_1593+378del
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Search 100 bp 3'