Canonical Allele Identifier: CA1572616529
Gene: TSLP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071796T= , CM000667.2:g.111071796T= GRCh38
NC_000005.9:g.110407494T= , CM000667.1:g.110407494T= GRCh37
NC_000005.8:g.110435393T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-95T= MANE Select ENSP00000339804.3:n.-95T=
ENST00000344895.3:c.-95T= ENSP00000339804.3:n.-95T=
ENST00000420978.6:c.35-129T= ENSP00000399099.2:n.35-129T=
NM_033035.4:c.-95T= NP_149024.1:n.-95T=
NR_045089.1:n.1439-129T=
NM_033035.5:c.-95T= MANE Select NP_149024.1:n.-95T=
NR_045089.2:n.1457-129T=
Search 100 bp 5'
Search 100 bp 3'