Canonical Allele Identifier: CA2767908729
Gene: TSLP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077892C>A , CM000667.2:g.111077892C>A GRCh38
NC_000005.9:g.110413590C>A , CM000667.1:g.110413590C>A GRCh37
NC_000005.8:g.110441489C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*1818C>A MANE Select ENSP00000339804.3:n.*1818C>A
ENST00000379706.4:c.*1818C>A ENSP00000427827.1:n.*1818C>A
NM_033035.4:c.*1818C>A NP_149024.1:n.*1818C>A
NM_138551.4:c.*1818C>A NP_612561.2:n.*1818C>A
NR_045089.1:n.3702C>A
NM_033035.5:c.*1818C>A MANE Select NP_149024.1:n.*1818C>A
NM_138551.5:c.*1818C>A NP_612561.2:n.*1818C>A
NR_045089.2:n.3720C>A
Search 100 bp 5'
Search 100 bp 3'