Canonical Allele Identifier: CA1572617110
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072206T= , CM000667.2:g.111072206T= GRCh38
NC_000005.9:g.110407904T= , CM000667.1:g.110407904T= GRCh37
NC_000005.8:g.110435803T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.171+145T= MANE Select ENSP00000339804.3:n.171+145T=
ENST00000344895.3:c.171+145T= ENSP00000339804.3:n.171+145T=
ENST00000420978.6:c.171+145T= ENSP00000399099.2:n.171+145T=
NM_033035.4:c.171+145T= NP_149024.1:n.171+145T=
NR_045089.1:n.1575+145T=
NM_033035.5:c.171+145T= MANE Select NP_149024.1:n.171+145T=
NR_045089.2:n.1593+145T=