Canonical Allele Identifier: CA1572617248
Gene: TSLP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072334G= , CM000667.2:g.111072334G= GRCh38
NC_000005.9:g.110408032G= , CM000667.1:g.110408032G= GRCh37
NC_000005.8:g.110435931G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+273G= MANE Select ENSP00000339804.3:n.171+273G=
ENST00000344895.3:c.171+273G= ENSP00000339804.3:n.171+273G=
ENST00000420978.6:c.171+273G= ENSP00000399099.2:n.171+273G=
NM_033035.4:c.171+273G= NP_149024.1:n.171+273G=
NR_045089.1:n.1575+273G=
NM_033035.5:c.171+273G= MANE Select NP_149024.1:n.171+273G=
NR_045089.2:n.1593+273G=
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