Canonical Allele Identifier: CA2674829036
Gene: TSLP HGNC NCBI

Linked Data

gnomAD v4: 5-111077160-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077163del , CM000667.2:g.111077163del GRCh38
NC_000005.9:g.110412861del , CM000667.1:g.110412861del GRCh37
NC_000005.8:g.110440760del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*1089del MANE Select ENSP00000339804.3:n.*1089del
ENST00000379706.4:c.*1089del ENSP00000427827.1:n.*1089del
NM_033035.4:c.*1089del NP_149024.1:n.*1089del
NM_138551.4:c.*1089del NP_612561.2:n.*1089del
NR_045089.1:n.2973del
NM_033035.5:c.*1089del MANE Select NP_149024.1:n.*1089del
NM_138551.5:c.*1089del NP_612561.2:n.*1089del
NR_045089.2:n.2991del
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