Canonical Allele Identifier: CA1572616476
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071725C= , CM000667.2:g.111071725C= GRCh38
NC_000005.9:g.110407423C= , CM000667.1:g.110407423C= GRCh37
NC_000005.8:g.110435322C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-166C= MANE Select ENSP00000339804.3:n.-166C=
ENST00000344895.3:c.-166C= ENSP00000339804.3:n.-166C=
ENST00000420978.6:c.35-200C= ENSP00000399099.2:n.35-200C=
NM_033035.4:c.-166C= NP_149024.1:n.-166C=
NR_045089.1:n.1439-200C=
NM_033035.5:c.-166C= MANE Select NP_149024.1:n.-166C=
NR_045089.2:n.1457-200C=