Canonical Allele Identifier: CA1572616814
Gene: TSLP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071985C= , CM000667.2:g.111071985C= GRCh38
NC_000005.9:g.110407683C= , CM000667.1:g.110407683C= GRCh37
NC_000005.8:g.110435582C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.95C= MANE Select ENSP00000339804.3:p.Thr32=
ENST00000344895.3:c.95C= ENSP00000339804.3:p.Thr32=
ENST00000420978.6:c.95C= ENSP00000399099.2:p.Thr32=
NM_033035.4:c.95C= NP_149024.1:p.Thr32=
NR_045089.1:n.1499C=
NM_033035.5:c.95C= MANE Select NP_149024.1:p.Thr32=
NR_045089.2:n.1517C=
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