Canonical Allele Identifier: CA2674829143
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077881del , CM000667.2:g.111077881del GRCh38
NC_000005.9:g.110413579del , CM000667.1:g.110413579del GRCh37
NC_000005.8:g.110441478del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*1807del MANE Select ENSP00000339804.3:n.*1807del
ENST00000379706.4:c.*1807del ENSP00000427827.1:n.*1807del
NM_033035.4:c.*1807del NP_149024.1:n.*1807del
NM_138551.4:c.*1807del NP_612561.2:n.*1807del
NR_045089.1:n.3691del
NM_033035.5:c.*1807del MANE Select NP_149024.1:n.*1807del
NM_138551.5:c.*1807del NP_612561.2:n.*1807del
NR_045089.2:n.3709del