Canonical Allele Identifier: CA801887073
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1229648319
gnomAD v3: 5-111071889-GTATGTTCCCTTTTGCCTTAC-G
gnomAD v4: 5-111071889-GTATGTTCCCTTTTGCCTTAC-G
MyVariant Identifiers: chr5:g.110407588_110407607del (hg19) chr5:g.111071890_111071909del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071893_111071912del , CM000667.2:g.111071893_111071912del GRCh38
NC_000005.9:g.110407591_110407610del , CM000667.1:g.110407591_110407610del GRCh37
NC_000005.8:g.110435490_110435509del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.3_22del MANE Select ENSP00000339804.3:p.Met1IlefsTer26
ENST00000344895.3:c.3_22del ENSP00000339804.3:p.Met1IlefsTer26
ENST00000420978.6:c.35-32_35-13del ENSP00000399099.2:n.35-32_35-13del
NM_033035.4:c.3_22del NP_149024.1:p.Met1IlefsTer26
NR_045089.1:n.1439-32_1439-13del
NM_033035.5:c.3_22del MANE Select NP_149024.1:p.Met1IlefsTer26
NR_045089.2:n.1457-32_1457-13del
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