Canonical Allele Identifier: CA1572617379
Gene: TSLP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072503T= , CM000667.2:g.111072503T= GRCh38
NC_000005.9:g.110408201T= , CM000667.1:g.110408201T= GRCh37
NC_000005.8:g.110436100T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.172-385T= MANE Select ENSP00000339804.3:n.172-385T=
ENST00000344895.3:c.172-385T= ENSP00000339804.3:n.172-385T=
ENST00000420978.6:c.172-385T= ENSP00000399099.2:n.172-385T=
NM_033035.4:c.172-385T= NP_149024.1:n.172-385T=
NR_045089.1:n.1576-385T=
NM_033035.5:c.172-385T= MANE Select NP_149024.1:n.172-385T=
NR_045089.2:n.1594-385T=
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