Canonical Allele Identifier: CA360602499
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071949T>G , CM000667.2:g.111071949T>G GRCh38
NC_000005.9:g.110407647T>G , CM000667.1:g.110407647T>G GRCh37
NC_000005.8:g.110435546T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.59T>G MANE Select ENSP00000339804.3:p.Leu20Ter
ENST00000344895.3:c.59T>G ENSP00000339804.3:p.Leu20Ter
ENST00000420978.6:c.59T>G ENSP00000399099.2:p.Leu20Ter
NM_033035.4:c.59T>G NP_149024.1:p.Leu20Ter
NR_045089.1:n.1463T>G
NM_033035.5:c.59T>G MANE Select NP_149024.1:p.Leu20Ter
NR_045089.2:n.1481T>G