Canonical Allele Identifier: CA1572616527
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071794G= , CM000667.2:g.111071794G= GRCh38
NC_000005.9:g.110407492G= , CM000667.1:g.110407492G= GRCh37
NC_000005.8:g.110435391G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-97G= MANE Select ENSP00000339804.3:n.-97G=
ENST00000344895.3:c.-97G= ENSP00000339804.3:n.-97G=
ENST00000420978.6:c.35-131G= ENSP00000399099.2:n.35-131G=
NM_033035.4:c.-97G= NP_149024.1:n.-97G=
NR_045089.1:n.1439-131G=
NM_033035.5:c.-97G= MANE Select NP_149024.1:n.-97G=
NR_045089.2:n.1457-131G=