Canonical Allele Identifier: CA1572616675
Gene: TSLP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071909C= , CM000667.2:g.111071909C= GRCh38
NC_000005.9:g.110407607C= , CM000667.1:g.110407607C= GRCh37
NC_000005.8:g.110435506C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.19C= MANE Select ENSP00000339804.3:p.Leu7=
ENST00000344895.3:c.19C= ENSP00000339804.3:p.Leu7=
ENST00000420978.6:c.35-16C= ENSP00000399099.2:n.35-16C=
NM_033035.4:c.19C= NP_149024.1:p.Leu7=
NR_045089.1:n.1439-16C=
NM_033035.5:c.19C= MANE Select NP_149024.1:p.Leu7=
NR_045089.2:n.1457-16C=
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