Canonical Allele Identifier: CA2674827866
Gene: TSLP HGNC NCBI

Linked Data

gnomAD v4: 5-111071916-TTC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071918_111071919del , CM000667.2:g.111071918_111071919del GRCh38
NC_000005.9:g.110407616_110407617del , CM000667.1:g.110407616_110407617del GRCh37
NC_000005.8:g.110435515_110435516del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.28_29del MANE Select ENSP00000339804.3:p.Leu10ValfsTer23
ENST00000344895.3:c.28_29del ENSP00000339804.3:p.Leu10ValfsTer23
ENST00000420978.6:c.35-7_35-6del ENSP00000399099.2:n.35-7_35-6del
NM_033035.4:c.28_29del NP_149024.1:p.Leu10ValfsTer23
NR_045089.1:n.1439-7_1439-6del
NM_033035.5:c.28_29del MANE Select NP_149024.1:p.Leu10ValfsTer23
NR_045089.2:n.1457-7_1457-6del
Search 100 bp 5'
Search 100 bp 3'