Canonical Allele Identifier: CA2674829012
Gene: TSLP HGNC NCBI

Linked Data

gnomAD v4: 5-111077028-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077030del , CM000667.2:g.111077030del GRCh38
NC_000005.9:g.110412728del , CM000667.1:g.110412728del GRCh37
NC_000005.8:g.110440627del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*956del MANE Select ENSP00000339804.3:n.*956del
ENST00000379706.4:c.*956del ENSP00000427827.1:n.*956del
NM_033035.4:c.*956del NP_149024.1:n.*956del
NM_138551.4:c.*956del NP_612561.2:n.*956del
NR_045089.1:n.2840del
NM_033035.5:c.*956del MANE Select NP_149024.1:n.*956del
NM_138551.5:c.*956del NP_612561.2:n.*956del
NR_045089.2:n.2858del
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