Canonical Allele Identifier: CA1572616552
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071819G= , CM000667.2:g.111071819G= GRCh38
NC_000005.9:g.110407517G= , CM000667.1:g.110407517G= GRCh37
NC_000005.8:g.110435416G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.-72G= MANE Select ENSP00000339804.3:n.-72G=
ENST00000344895.3:c.-72G= ENSP00000339804.3:n.-72G=
ENST00000420978.6:c.35-106G= ENSP00000399099.2:n.35-106G=
NM_033035.4:c.-72G= NP_149024.1:n.-72G=
NR_045089.1:n.1439-106G=
NM_033035.5:c.-72G= MANE Select NP_149024.1:n.-72G=
NR_045089.2:n.1457-106G=